Research Associate Jobs

Research Associate

Texas A&M University

College Station, TX

The Research Associate will design and execute laboratory protocols including cell isolation and molecular biology techniques, supervise students, manage lab inventory, and maintain animal research care.

Requisition No: 883197 Agency: Commerce Working Title: 883197 - RESEARCH ASSOCIATE - 40050035 1 Pay Plan: Career Service Position Number: 40050035 Salary: $45,000.00-$47,900.00 Posting Closing Date: 09/21/2026 Total Compensation Estimator Tool JOB TYPE: FULL TIME / CAREER SERVICE POSITION LOCATION: Tallahassee, FL (relocation benefits are not available for this position) Research Associate OPEN COMPETITIVE www.floridajobs.org/ Your Specific Responsibilities: Under general supervision of the Economic Consultant-SES, this position involves the development of industry and employment projections for the State of Florida and various sub-state areas. This position involves forecasting both industry and occupational employment trends at the state and local level as part of the data production process. This position performs work compiling, coding, analyzing, and conducting research on employment and wage data for use in the preparation of current occupational employment estimates (staffing patterns) and occupational wages for the State of Florida, Metropolitan Statistical Areas (MSA), and Balance-Of-State areas (BOS). Produces occupational employment and wage estimates tables and forecasts for the State of Florida and numerous sub-state areas using the MicroMatrix system to convert industry projections into occupational projections. This may involve utilizing computer programs and/or advanced software application programs to assist in producing projections. Associate is responsible for generating OES survey employment and wage estimates tables for the Floridajobs.org and Florida Insight websites. Files are produced for Florida statewide and all sub-state areas on an annual basis following the receipt of new survey estimates from the U.S. Bureau of Labor Statistics (BLS). Associate is also responsible for preparing detailed industry staffing pattern files for all workforce regions and other sub-state areas, as needed, for use in the development of occupational employment projections. Reviews occupational estimates on an annual basis. Provides technical assistance for the maintenance and updating of the Local Employment & Wage Information System (LEWIS). Produces, reviews, screens and publishes employment and wage estimates using LEWIS. Imports new estimates data from BLS into LEWIS. Responds and provides data for all LEWIS requests. Serves as Program Specialist. Updates and maintains Occupational Employment Statistics survey database files for Florida businesses selected by the Bureau of Labor Statistics. Serves on address refinement team as needed to ensure updates are made with proper usage of Melissa Data. Utilizes the internet to complete search for current address and updates business contact information as needed. Analyzes employment and wage data giving special attention to the data highlighted for review when being entered in the database. Reviews quality assurance edits showing unusual occupations, high and low wages, missing, and dependent occupations. Reviews, verifies, and makes necessary corrections to the data entered. Explains any unusual variances in staffing patterns and/or wages in the comment’s module. Collects, compiles, analyzes, and reviews occupational employment and wage survey data for assigned survey units and their employment. Analyzes and edits survey responses, assigns occupational codes to the job descriptions reported by employers, and enters the data into the Occupational Employment Statistics (OES) computer software system. Reviews and processes all electronic survey responses with significant employment and occupations using the BLS provided “Auto-batch” utility. Utilizes the internet to conduct research on businesses. Verification of atypical data with the employer and the addition of written comments on the survey data file may be necessary. Reviews and corrects North American Industry Classification System codes assigned to individual establishments on the Occupational Employment Statistics survey sample. Research and investigates businesses which indicate they are classified incorrectly on the Quarterly Census of Employment & Wages database. After extensive analysis and review, makes any changes to the Occupational Employment Statistics survey database to reflect the best North American Industry Classification System code for all businesses selected for the Occupational Employment Statistics survey sample by Bureau of Labor Statistics. Works closely with other units within and outside of Labor Market Statistics . Prepares economic reports and other labor market information with explanations, analyses, and general correspondence as needed. This may require the use of advanced computer software and/or the development of customized computer programs to produce these special reports, charts, graphs, and/or presentations of data for the user. Assists with responding to special requests for employment and wage information, which may be atypical from the standard reports produced by the OES program. This requires the use of the LEWIS software system to generate occupational employment and wage estimates for specific industries or geographic locations as requested by data users. Assist in industry and occupational forecasts for the State of Florida and numerous sub-state areas for use in the development of supply/demand. Performs other duties as required. Required Knowledge, Skills, and Abilities: Knowledge and proficiency using Microsoft Office applications Ability to collect and analyze data. Ability to navigate the internet and conduct research Knowledge of statistical methods and economic principles Knowledge of North American Industry Classification System (NAICS) and the Standard Occupational Classification (SOC) coding taxonomies. Advanced software programs -Tableau, R-Suite, MS SQL Server, SQL Reporting services, understanding of SQL database management and architecture. Knowledge of economic theory and principles. Qualifications: As a condition of pre-employment eligibility, a Level 2 security background screening is required, which consists of fingerprinting and a check of local, state, and national law enforcement records. Minimum: Duties and responsibilities of this position must be performed at the official work site of the Department. Preferred : Bachelor's degree from an accredited college or university in Economics, Statistics, or Math or related social science. Four years of experience in research and data analysis. Experience using spreadsheet applications. Knowledge of advanced software (i.e., R, SAS, Tableau, SQL) Pay: $45,000.00 - $47,900.00 annually Our Organization and Mission: FloridaCommerce works across the state to support Florida’s economy, robust and talented workforce, and our local communities. We are dedicated to making a stronger and more resilient Florida, so our businesses, communities, and workforce are better prepared to withstand future economic slowdowns and natural disasters. In collaboration with our partners, we salute our nation’s veterans and are honored to have the opportunity to support them and their family members by encouraging them to apply at FloridaCommerce for positions that fit their skill sets. FloridaCommerce is an Equal Opportunity Employer/Program. Auxiliary aids and services are available upon request to individuals with disabilities. (TTY/TDD 1-800-955-8771 or the Florida Relay Service – 711.) Let our mission become yours. To find out more about us, click on the link: http://www.floridajobs.org/ The Work You Will Do: The Research Associate is a member of the Labor Market Statistics team of the Division of Workforce Services. This position is critical to meeting contract deliverables with the U.S. Bureau of Labor Statistics and involved in the development of industry and employment projections for the State and substate areas. This position involves forecasting both industry and occupational employment trends at the state and local level as part of the data production process. A thorough working knowledge of economic theory and principles, knowledge of statistics, the methods of data collection, the ability to collect and analyze data, and a broad knowledge of microcomputers, software, and programming are required. This position involves work compiling, coding, analyzing, and conducting research on employment and wage data for use in the preparation of current occupational employment estimates (staffing patterns) and occupational wages for the State of Florida, Metropolitan Statistical Areas (MSA), and Balance-Of-State areas (BOS). These estimates are the primary source for developing occupational employment projections used for program planning by the education and job training community. No leadership responsibilities. The Difference You Will Make: This position is part of a team that produces the most detailed occupational employment and wage data for the State. These data are used to determine average employment and wages which are used by Florida Commerce leadership, workforce and economic development agencies, employers, and educational institutions. FloridaCommerce is a fast-paced work environment in which critical thinking and prioritizing are a must. How You Will Grow: FloridaCommerce encourages its employees to constantly innovate and seek efficiencies. Trainings are made available throughout the year and on request with the Office of Training and Development within the Bureau of Human Resource Management. In accordance with our Vision and Mission, the employee: Furthers Florida’s economic vision by providing support that enhances the economy and develops, safe, and healthy communities. Meets customer/client expectations with an emphasis on responsiveness, quality, quantity, and timeliness of work. Provides information clearly, accurately, and succinctly; and exhibits good listening skills. Works collaboratively to optimize the effectiveness of FloridaCommerce’s available resources and tools. Uses knowledge acquired through education, training, or experience to complete tasks. These expectations are for all our employees, and you will be expected to model these as a leader. We believe in supporting and encouraging you as you take on important and often complex projects while offering you the opportunity to gain valuable experience. Where You Will Work Tallahassee is Florida’s Capital City and continues to grow by attracting development and new businesses. T allahassee is a mid- sized city in the heart of Florida’s Big Bend. FloridaCommerce’s main office is located in Downtown Tallahassee, the political epicenter that draws in visitors each year to visit the state’s Capitol. Each spring, the legislative session opens, and people pour in to see the Florida Legislature perform business and approve the state’s annual budget. Being in Tallahassee will guarantee you an experience vibrant with a unique experience, professional growth, entertainment, and culture. Tallahassee is: Known for its beautiful parks, rolling hills and oak trees, canopied roads, hotels, dining, museums, arts, music, and natural resources ( https://talgov.com/ ) Home to major college campuses, Florida State University (FSU), Florida A & M University (FAMU) and Tallahassee Community College (TCC). Approximately 22 miles from the nearest beach ( https://choosetallahassee.com/beaches-near-tallahassee/ ) Within a state having no state income tax for residents of Florida WORKING FOR THE STATE OF FLORIDA HAS BENEFITS! * State Group Insurance coverage options+ ( health, life, dental, vision, and other supplemental option ) * Retirement plan options, including employer contributions ( www.myfrs.com ) * Nine paid holidays and a Personal Holiday each year * Annual and Sick Leave Benefits * Student Loan Forgiveness Program ( Eligibility required ) * Flexible Spending Accounts * Tuition Fee Waivers (Accepted by major Florida colleges/universities) * Ongoing comprehensive training provided * Career Growth * Highly skilled, professional environment For a more complete list of benefits, visit www.mybenefits.myflorida.com . * We care about the success of our employees. * We are always improving our technology, our tools, our customer’s experiences, and ourselves. * A rewarding experience for reliable, compassionate, and professional employees. Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (1-866-663-4735). Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation. The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act. VETERANS’ PREFERENCE. Pursuant to Chapter 295, Florida Statutes, candidates eligible for Veterans’ Preference will receive preference in employment for Career Service vacancies and are encouraged to apply. Certain service members may be eligible to receive waivers for postsecondary educational requirements. Candidates claiming Veterans’ Preference must attach supporting documentation with each submission that includes character of service (for example, DD Form 214 Member Copy #4) along with any other documentation as required by Rule 55A-7, Florida Administrative Code. Veterans’ Preference documentation requirements are available by clicking here . All documentation is due by the close of the vacancy announcement.

Research Associate

Agilent Technologies

US-CO-Boulder

Job Description Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek ---- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com. We are seeking a Research Associate to join the team. The candidate will be responsible for conducting process R&D activities for developing and optimizing enzymatic ligation and downstream processes at the lab scale for tech transfer to large-scale oligonucleotide production. This includes assisting in developing and optimizing ligation process, methods, and techniques in preparing, separating, purifying, analyzing, quantifying, and resolving oligonucleotide process components and objectives. Key responsibilities include: · Studying and implementing R&D project objectives and targets related to chemical and engineering requirements of oligonucleotide production processes · Apply knowledge and laboratory experience in chemistry and analytical testing by implementing strategies and optimizing chemical reactions, methods and processes · Execute process development experiments and activities related to enzymatic ligation and downstream processing of complex oligonucleotides · Complete experimental notebooks and records adhering to standard operating procedures (SOP's) and current good manufacturing practices to maintain compliance integrity (cGMP) · Participate in cross-functional teams and support project teams in all stages of oligonucleotide research and development Qualifications Required: · Bachelor’s in chemistry, biochemistry, chemical engineering, biochemical engineering or related science discipline · Two years of industrial experience post-graduation in a pharmaceutical environment · Knowledge and understanding of process chemistry and development · Ability to work both independently and in a team setting on a variety of projects Desired: · Master’s Degree preferred · Knowledge of enzymatic manipulation of DNA/RNA and biocatalysis · Detail and results oriented with experience in experimental plan and execution, data analysis, and documentation · General proficiency with tools, systems, and procedures Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least September 1, 2026 or until the job is no longer posted. The full-time equivalent pay range for this position is $76,080.00 - $118,875.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility. Travel Required: No Shift: Day Duration: No End Date Job Function: R&D Life sciences instruments, diagnostics, and applied chemistry solutions provider. Headquartered in Santa Clara, CA. agilent.com

BS or MS in a relevant life science field, 1–2 years of research experience, molecular biology techniques including PCR, electrophoresis, and DNA purification, plus strong mathematical, statistical, and experimental skills.

No Description

Senior Research Associate

Research Compliance Office of the Texas A&M University System

College Station, TX

The Senior Research Associate will design, plan, conduct, and coordinate agricultural field operations, including planting and harvesting, while supervising undergraduate students and maintaining agricultural equipment.

Research Associate II

Joulé

Oro Valley, AZ

The Research Associate II will conduct research and laboratory experimentation to support IHC and molecular detection kit development, ensuring compliance with GMP and GLP standards. Key focus includes: Conduct research and laboratory experimentation to support IHC and molecular detection kit development.

Postdoctoral Research Associates - NRC Research Associateship Programs

The National Academies of Science, Engineering, and Medicine

Remote

The National Academies of Sciences, Engineering, and Medicine maintain a database of more than a thousand active research opportunities and administer postdoctoral and senior research awards at participating federal laboratories and affiliated institutions at locations throughout the U.S. and abroad. We are seeking highly qualified candidates who hold, or anticipate earning a Ph.D., Sc.D., M.D., or D.V.M. in a variety of fields of science or engineering. Senior research awards are designated for those with >5 years since earning their degree. Research Associates have the opportunity to: Design and conduct an original, independent research project in an area compatible with the interests of the sponsoring laboratory Enhance their visibility in their field through a nationally-recognized, competitive award Devote full-time effort to mission-driven research that contributes to national priorities Access the excellent and often unique facilities of the federal research enterprise Collaborate with leading scientists and engineers at the sponsoring laboratories Award benefits include: Competitive monthly stipend (base stipend varies by host laboratory and may be higher based on experience; refer to research opportunity description for amount) Health insurance (including dental and vision) Relocation assistance for awardees who will be on tenure for at least six months and who at the time of award reside more than 50 miles from the host laboratory Professional travel allowance Qualified applicants will receive consideration without regard to race, creed, color, age, gender identity, or national origin. Citizenship eligibility varies among the sponsoring laboratories and will be indicated in the research opportunity. NEXT DEADLINE: Apply by November 2nd! Visit www.nas.edu/rap for further program details, eligibility, required application components, and guidance for submitting an application!

Clinical Research Associate

ICON plc

US, Blue Bell (ICON)

Clinical Research Assoicate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland. iconplc.com

Clinical Research Associate

ICON plc

United States of America, US

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. Job Advert Posting We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile Bachelor's degree in a scientific or healthcare-related field. Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland. iconplc.com

The Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards. The Clinical Research Associate r ole is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders. The Clinical Research Associate is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner, and other members of the study team, as required, in activities associated with the set-up, running and close out of sites in a clinical trial. Responsible for investigator site management and monitoring for assigned sites: Clinical Trial Monitoring Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices, and Pfizer standards to achieve project goals, timelines and quality Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site initiation through to database lock, ensuring relevant timelines and quality deliverables are met During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks Attend investigator meetings when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level Conduct remote assessment of e diary data Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the Study Monitoring Plan, SOPs and commensurate with emerging issues and technologies. Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics Identify and resolve investigator site issues within required timeframes; agree and develop corrective and preventative actions with investigator and site personnel to close open issues and to prevent recurrence/persistence of issues Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage conditions, and destruction activities. Support database release as needed May undertake the responsibilities of an unblinded monitor where appropriate Clinical/Scientific and Site Monitoring Risk: Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team Interact with investigator site health care professionals in a manner which enhances Pfizer’s credibility, scientific leadership and in order to facilitate Pfizer’s clinical development goals Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators Drive Quality Event submission and remediation, when applicable Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicable QUALIFICATIONS Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent Knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations Monitoring Experience: Minimum 1-year relevant experience in clinical research site monitoring and management Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases Global clinical trial experience preferred Must be fluent in English and in the native language(s) of the country they will work in Demonstrated knowledge of clinical research and development processes and ability to gain command of process details Demonstrated knowledge of global and local regulatory requirements Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.) Demonstrated knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s) Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery Ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial Ability to evaluate, interpret and present complex issues and data to support risk management and mitigation Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Significant travel (60-80%) within area is required. May require some international travel and some weekend travel Valid driver’s license and passport required 
The annual base salary for this position ranges from $68,600.00 to $114,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.



This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.


 Relocation assistance may be available based on business needs and/or eligibility. 
 Candidates must be authorized to be employed in the U.S. by any employer. U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future. 
 Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. 
 EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States. Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. 
 To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers . 
Medical


Senior Research Associate

Natera

Austin, TX

. Company: Natera. Responsibilities: The Senior Research Associate will design and execute experimental workflows for oncology product development and NGS assay validation. They will also maintain detailed laboratory records and coordinate across internal teams to ensure timely study execution.

Research Associate - Electrophysiology

Baylor College of Medicine

Houston, TX

Monday - Friday, 8 a.m. - 5 p.m. Summary The St-Pierre lab develops and applies new tools for monitoring and interrogating brain activity with millisecond-timescale temporal resolution. We seek an energetic team member to lead our efforts to characterize and apply new light-responsive proteins in vitro and in vivo. The Research Associate will work on two types of tools: (1) genetically encoded voltage indicators (GEVIs), fluorescent biosensors that report voltage as changes in brightness, and (2) optogenetic silencers, light-gated channels that inhibit neuronal firing. Characterization of these tools requires simultaneous electrophysiological recordings and optical excitation/imaging. This position provides exciting opportunities to work with the latest optical technologies and develop new skills in two-photon voltage Job Duties Culture mammalian cells Prepare brain slices, dissociated neurons, or both Conduct experiments that combine electrophysiology and either optogenetic activation or optical imaging (multi-photon fluorescence microscopy) Maintain reagent and tool supply related to the experiments Maintain an electrophysiological rig, and troubleshooting if needed Analyze data using commercial software or customized data pipelines Teach techniques, procedures, and experimental design to other members of the lab Communicate research results in group meetings, national or international conferences Plan, direct and conduct research experiments Evaluate and analyze data Develop research techniques and perform applications required for specific research projects May conduct literature searches and summarize information in an appropriate format for a particular study Document results of experiments and report to principal investigators May supervise, schedule and coordinate the activities of less experienced research staff Perform other job related duties as assigned Minimum Qualifications Master's degree in Basic Science or a related field. Experience in lieu of degree will not be accepted. Three years of relevant experience typically as a Research Assistant, Research Technician or Postdoctoral Fellow/Associate. Department Specific Criteria Must have experience with performing electrophysiology in dissociated neurons, brain slices or both Must have experience with dissecting rat cortical, hippocampal neurons, or both Must have experience maintaining an electrophysiology rig Preferred Qualifications Doctoral degree Ability to express transgenes in neurons of brain slices using viruses and/or in utero electroporation Experience with imaging neural activity (e.g. voltage or calcium) in brain slices or in vivo, using 1P and/or 2P imaging Work Authorization Requirement: This position is not eligible for visa sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment. Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.

Clinical Research Associate

ICON plc

United States of America, US

Clinical Research Associate - Multi TA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: Advanced degree in a relevant field such as life sciences, nursing, or medicine. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland. iconplc.com

POSTDOCTORAL RESEARCH ASSOCIATE

Texas A&M University, Microbial Pathogenesis and Immunology Department

Bryan, TX

POSTDOCTORAL RESEARCH ASSOCIATE position is available immediately to join the research group of Dr. Jeffrey D. Cirillo at Texas A&M University, developing REFtb, a rapid tuberculosis diagnostic platform based on the M. tuberculosis enzyme BlaC and fluorogenic substrate chemistry. Selected individual will be responsible for developing and optimizing REFtb diagnostic reagents, including expression, purification, and kinetic characterization of BlaC and related beta-lactamases, and evaluation of fluorogenic substrate selectivity and assay performance in clinical sample matrices. Ph.D. required and a record of productive experience in enzymology, assay optimization, and/or reagent stabilization (lyophilization) preferred. Interested applicants should apply on-line at https://bit.ly/3SIzTSz and send curriculum vitae and names and addresses of three references postmarked by September 9, 2026 (or until a suitable candidate is found), to Dr. Jeffrey Cirillo, Dept. of Microbial Pathogenesis and Immunology, Texas A&M University School of Medicine, 8447 John Sharp Parkway, 3350 Medical Research and Education Bldg. II, Bryan, TX 77807-3260. FAX: 979-436-0360; email: jdcirillo@tamu.edu. Texas A&M University is an Equal Opportunity/Affirmative Action/Veterans/Disability Employer. Contact: Dr. Jeffrey Cirillo, Telephone: 979-436-0343 for additional information.

Clinical Research Associate

ICON plc

US Blue Bell ICON

Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland. iconplc.com

Investment Research Associate

Seaport Global

United States

Seaport Research Partners Overview Seaport Research Partners (“SRP”) is a rapidly expanding, innovative sell -side research platform. SRP empowers self-driven analysts/strategists by reshaping economics and delivering a fully integrated solution to support, enhance and grow their franchise, allowing them to focus exclusively on producing the customized and differentiated research that matters most to clients. Seaport’s platform is increasingly attracting top analysts and buy-side customers alike. Twenty-four (24) senior analysts/strategists have joined the platform and bring an average of 20 years’ experience, most with prior experience at bulge bracket firms and many receiving industry recognition such as II rankings. SRP operates as a division of Seaport Global Securities, which brings established global client relationships, access to over 4,000 opened institutional accounts, 210 senior salespeople & traders across the cap structure, asset management, global equity and debt capital markets, a full suite of corporate access services including multi-sector and niche conferences, fixed income & derivatives research and investment banking. Seaport Global’s offices throughout the US as well as London provide a superior network and deep infrastructure. Opportunity We are looking for investment associates to join our equity research team. This will be a remote, work from home opportunity. Qualifications: Minimum of one to five years’ work experience in either investment research, banking, accounting or consulting. Majors in computer science, engineering, finance or accounting preferred. Strong quantitative and excel skills. Python or other programming skills and experience. Ability to work in a team environment and help problem solve. Entrepreneurial mindset with a commitment to excellence and contributing to the team’s success. Ability to work independently in a fast-paced team environment. Strong communication, writing, and presentation skills. To apply, please submit resume and the following information to Originally posted on Himalayas

Postdoctoral Research Associate

University of Nebraska Medical Center

Omaha, NE

Dr. Jian Xie’s laboratory in the Department of Pathology, Microbiology, and Immunology at the University of Nebraska Medical Center (UNMC), a nationally recognized institution ranked Tier 1 in Primary Care and Tier 2 in Research, is seeking an outstanding candidate for a Postdoctoral Research Associate position. The successful candidate will investigate the roles of cell surface RNAs and glycoRNAs in viral entry and infection, with a particular emphasis on oncogenic viruses such as human papillomavirus (HPV). Although RNA was traditionally considered to be confined to the nucleus and cytoplasm, recent studies have revealed that a subset of RNAs is glycosylated and displayed on the cell surface (cell surface glycoRNAs) ( Cell , 2021; Cell , 2024; Nature , 2026). These discoveries have further led to the unexpected finding that RNA-binding proteins (RBPs) are common components of the cell surface ( Cell , 2025; Nature Biotechnology , 2025; Molecular Cell , 2025). Positioned at the interface between the cell and its environment, cell surface RNAs (csRNAs) and cell surface RNA-binding proteins (csRBPs) are strategically situated to regulate fundamental biological processes, including cell–cell communication, pathogen recognition, and receptor-mediated signaling. Emerging evidence suggests that these newly identified surface molecules form functional complexes with important roles in immune regulation and cancer biology ( Cell , 2024; Nature , 2025). However, the mechanistic principles governing their functions during pathogen infection remain unknown. The Xie laboratory studies virus–host interactions in viral infection, cancer, and innate immunity ( PNAS , 2026; PNAS , 2025; Science Advances , 2021; Cell Reports , 2020). Our recent work indicates that csRNAs and csRBPs are critical determinants of HPV infection and may constitute a previously unrecognized class of viral entry receptors. This research is supported by an NIH R35 award and is conducted through strong collaborations with leading laboratories at Yale University and Harvard University. https://www.ncbi.nlm.nih.gov/myncbi/jian.xie.3/bibliography/public/ The successful candidate will receive individualized, mentor-guided training and gain access to emerging concepts, experimental systems, and technologies developed by the laboratory and its collaborators. The candidate will design and conduct studies involving RNA and protein biochemistry, virology, cell biology, and molecular biology. Responsibilities will include experimental design; data collection, analysis, and interpretation; presentation of findings at institutional, regional, national, and international scientific meetings; preparation of manuscripts and grant applications; and mentoring of graduate students and other junior researchers, as appropriate. The ideal candidate will be highly motivated, creative, collaborative, and intellectually independent, with a strong interest in developing innovative hypotheses and experimental approaches.

Clinical Research Associate II / Senior Clinical Research Associate

ICON plc

Regional United States PRA, US

North America | Remote | Sponsor-Dedicated (FSP) Opportunities ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities. About the Opportunity As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide. Depending on your experience level, you may: Conduct site qualification, initiation, routine monitoring, and close-out visits Ensure protocol compliance, patient safety, data quality, and regulatory adherence Build strong relationships with investigative sites and key stakeholders Identify and proactively resolve site and study issues Collaborate with cross-functional teams to support successful study delivery Support inspection readiness and high-quality study execution Mentor and guide less experienced CRAs (Senior CRA level) What We're Looking For CRA II Bachelor's degree in a scientific, healthcare, or related field Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices Ability to work independently while collaborating effectively across teams Senior CRA Significant clinical monitoring experience across multiple studies and sites Advanced knowledge of clinical trial processes, regulations, and site management Proven ability to manage priorities and drive study quality independently Experience mentoring or supporting other CRAs is advantageous For all applicants Strong communication and relationship-building skills Willingness to travel as required Passion for advancing clinical research and improving patient outcomes When you join ICON Strategic Solutions, you gain the best of both worlds: Work within dedicated sponsor environments Build expertise with leading global pharmaceutical and biotechnology companies Access diverse opportunities across multiple therapeutic areas Benefit from ICON's global scale, career development, and support network Join a culture focused on innovation, collaboration, and patient impact Competitive compensation and benefits package Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland. iconplc.com

Clinical Research Associate

Lifelancer

United States

Job Title: Clinical Research Associate Job Location: Spain Remote Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. The CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained. Identify gaps and areas for improvement and propose CAPA. Supports start-up and provides local expertise. SSU experience is considered a plus CRA activities Perform feasibility, site identification, selection and evaluation, supporting initial list of sites and recruitment targets Provides protocol and related study training to assigned sites. Conducts monitoring (pre-study, initiation, routine monitoring and closeout visits per monitoring plan and applicable SOPs Conducts co-monitoring visits, if required Completes monitoring visit reports in accordance with ICH-GCP, BeOne Medicines standards and SOP Manages sites and site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations Ensure inspection readiness of the study and sites Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.) Attends disease indication project specific training and general CRA training as required Facilitate Study Oversight Visits (SOVs), site audits and/or inspections, as required Evaluates the quality and integrity of site practices – escalating quality and/or GCP issues with Investigators and internal team as appropriate. Anticipate and identify site issues; propose corrective and preventative actions; identify gaps and utilize opportunities. Constantly strive for operating excellence, question status-quo and promote innovation. Education Required: BS in a relevant scientific discipline and minimum of 2 years of monitoring experience. Experience in oncology global trials preferred Other Qualifications: Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines At least 2 years of (CRA) monitoring experience in the pharmaceutical or CRO industry Experience in oncology/hematology trials preferred Excellent communication and interpersonal skills Excellent organizational skills and ability to prioritize and multi-task Fluent in English & Spanish (writing and speaking) Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook Travel: up to 60% Salary Range EU: 46,100.00 EUR - 57,600.00 EUR Global Competencies When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Originally posted on Himalayas