Clinical Trial Associate Jobs for OPT Students
Clinical Trial Associate jobs are a strong fit for F-1 OPT students with degrees in life sciences, public health, or biomedical fields. Most CTA roles qualify as STEM OPT-eligible, giving you up to 36 months of work authorization. Employers in pharma, biotech, and CROs actively hire for this entry-level research operations role.
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Discover Vanderbilt University Medical Center: Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of individuals who come to work each day with the simple aim of changing the world. It is a place where your expertise will be valued, your knowledge expanded, and your abilities challenged. Vanderbilt Health is committed to an environment where everyone has the chance to thrive and where your uniqueness is sought and celebrated. It is a place where employees know they are part of something that is bigger than themselves, take exceptional pride in their work and never settle for what was good enough yesterday. Vanderbilt’s mission is to advance health and wellness through preeminent programs in patient care, education, and research.
Organization:
Pediatric Infectious Disease
Job Summary:
This position is with the VISPR Program, formerly called the Halasa/Chappell Lab, jointly led by Drs Natasha Halasa and Jim Chappell, within the Division of Pediatric Infectious Diseases at Vanderbilt University Medical Center. Our laboratory research concentrates on the etiology, epidemiology, prevention, and pathobiology of infectious diseases.
This position performs a variety of duties involved in the collection, interpretation, and documentation of data in support of clinical trials with regular guidance. Assists in ensuring adherence to protocols, appropriate regulations, and deadlines.
KEY RESPONSIBILITIES
Preparation and Coordination:
- Knowledgeable of protocols in order to determine specific criteria for eligibility or exclusion.
- Sets up timeline of tests and required procedures.
- Prepares kits for procedures and labels tubes with specific times and dates for collection.
- Assists with monitoring compliance with protocol and regulations.
- Informs nurse of tests and procedures as needed.
- Conducts follow-up of study patients.
- Ensures deadlines are met for study.
Research Data Collection:
- Abstracts and records all patient data essential to the study onto required case report forms.
- Inputs all pertinent patient data into database accurately.
- Collects and monitors all study patients records to document treatments and outcomes as required by the protocol.
- Reports all adverse reactions according to VUMC and protocol guidelines.
- Calls or sends questionnaires to patient to check outcomes, survival rate, and quality of life.
Maintaining Records:
- Ensures complete source documentation in record.
- Meets with and assists in response to sponsors and monitors to ensure compliance with protocol and applicable regulations.
- Examine data and records to ensure compliance with protocol.
TECHNICAL CAPABILITIES
- Laboratory Practices (Novice): Possesses sufficient fundamental proficiency to successfully demonstrate laboratory practices in practical applications of moderate difficulty. Generally works under the direction of others while accomplishing assignments.
- Medical Records Management (Novice): Knowledge of how and where to store and maintain basic records associated with job assignments.
- Research Administration (Novice): Knowledgeable on all phases in the lifecycle of a sponsored research project. Well versed in and able to assist researchers in reducing compliance risks and assisting in routine and specialized processes.
Our Academic Enterprise is one of the nation’s longest serving and most prestigious academic medical centers. Through its historic bond with Vanderbilt University and integral role in the School of Medicine, Vanderbilt Health cultivates distinguished research and educational programs to advance a clinical enterprise that provides compassionate and personalized care and support for millions of patients and family members each year.
World-leading academic departments and comprehensive centers of excellence pursue scientific discoveries and transformational educational and clinical advances across the entire spectrum of health and disease.
Aligning with Vanderbilt Health’s Strategic Directions, the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff.
Core Accountabilities:
- Organizational Impact: Delivers job responsibilities that impact own job area/team with some guidance.
- Problem Solving/ Complexity of work: Uses existing procedures, research and analysis to solve standard job related problems that may require some judgement.
- Breadth of Knowledge: Requires subject matter knowledge within a professional area to meet job requirements.
- Team Interaction: Individually contributes to project/ work teams.
Core Capabilities:
Supporting Colleagues:
- Develops Self and Others: Continuously improves own skills by identifying development opportunities.
- Builds and Maintains Relationships: Seeks to understand colleagues priorities, working styles and develops relationships across areas.
- Communicates Effectively: Openly shares information with others and communicates in a clear and courteous manner.
Delivering Excellent Services:
- Serves Others with Compassion: Invests time to understand the problems, needs of others and how to provide excellent service.
- Solves Complex Problems: Seeks to understand issues, solves routine problems, and raises proper concerns to supervisors in a timely manner.
- Offers Meaningful Advice and Support: Listens carefully to understand the issues and provides accurate information and support.
Ensuring High Quality:
- Performs Excellent Work: Checks work quality before delivery and asks relevant questions to meet quality standards.
- Ensures Continuous Improvement: Shows eagerness to learn new knowledge, technologies, tools or systems and displays willingness to go above and beyond.
- Fulfills Safety and Regulatory Requirements: Demonstrates basic knowledge of conditions that affect safety and reports unsafe conditions to the appropriate person or department.
Managing Resources Effectively:
- Demonstrates Accountability: Takes responsibility for completing assigned activities and thinks beyond standard approaches to provide high-quality work/service.
- Stewards Organizational Resources: Displays understanding of how personal actions will impact departmental resources.
- Makes Data Driven Decisions: Uses accurate information and good decision making to consistently achieve results on time and without error.
Fostering Innovation:
- Generates New Ideas: Willingly proposes/accepts ideas or initiatives that will impact day-to-day operations by offering suggestions to enhance them.
- Applies Technology: Absorbs new technology quickly; understands when to utilize the appropriate tools and procedures to ensure proper course of action.
- Adapts to Change: Embraces changes by keeping an open mind to changing plans and incorporates change instructions into own area of work.
Position Qualifications:
Responsibilities:
Certifications:
Work Experience:
Relevant Work Experience
Experience Level:
Less than 1 year
Education:
Associate's
Vanderbilt Health is committed to fostering an environment where everyone has the chance to thrive and is committed to the principles of equal opportunity. EOE/Vets/Disabled.

Discover Vanderbilt University Medical Center: Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of individuals who come to work each day with the simple aim of changing the world. It is a place where your expertise will be valued, your knowledge expanded, and your abilities challenged. Vanderbilt Health is committed to an environment where everyone has the chance to thrive and where your uniqueness is sought and celebrated. It is a place where employees know they are part of something that is bigger than themselves, take exceptional pride in their work and never settle for what was good enough yesterday. Vanderbilt’s mission is to advance health and wellness through preeminent programs in patient care, education, and research.
Organization:
Pediatric Infectious Disease
Job Summary:
This position is with the VISPR Program, formerly called the Halasa/Chappell Lab, jointly led by Drs Natasha Halasa and Jim Chappell, within the Division of Pediatric Infectious Diseases at Vanderbilt University Medical Center. Our laboratory research concentrates on the etiology, epidemiology, prevention, and pathobiology of infectious diseases.
This position performs a variety of duties involved in the collection, interpretation, and documentation of data in support of clinical trials with regular guidance. Assists in ensuring adherence to protocols, appropriate regulations, and deadlines.
KEY RESPONSIBILITIES
Preparation and Coordination:
- Knowledgeable of protocols in order to determine specific criteria for eligibility or exclusion.
- Sets up timeline of tests and required procedures.
- Prepares kits for procedures and labels tubes with specific times and dates for collection.
- Assists with monitoring compliance with protocol and regulations.
- Informs nurse of tests and procedures as needed.
- Conducts follow-up of study patients.
- Ensures deadlines are met for study.
Research Data Collection:
- Abstracts and records all patient data essential to the study onto required case report forms.
- Inputs all pertinent patient data into database accurately.
- Collects and monitors all study patients records to document treatments and outcomes as required by the protocol.
- Reports all adverse reactions according to VUMC and protocol guidelines.
- Calls or sends questionnaires to patient to check outcomes, survival rate, and quality of life.
Maintaining Records:
- Ensures complete source documentation in record.
- Meets with and assists in response to sponsors and monitors to ensure compliance with protocol and applicable regulations.
- Examine data and records to ensure compliance with protocol.
TECHNICAL CAPABILITIES
- Laboratory Practices (Novice): Possesses sufficient fundamental proficiency to successfully demonstrate laboratory practices in practical applications of moderate difficulty. Generally works under the direction of others while accomplishing assignments.
- Medical Records Management (Novice): Knowledge of how and where to store and maintain basic records associated with job assignments.
- Research Administration (Novice): Knowledgeable on all phases in the lifecycle of a sponsored research project. Well versed in and able to assist researchers in reducing compliance risks and assisting in routine and specialized processes.
Our Academic Enterprise is one of the nation’s longest serving and most prestigious academic medical centers. Through its historic bond with Vanderbilt University and integral role in the School of Medicine, Vanderbilt Health cultivates distinguished research and educational programs to advance a clinical enterprise that provides compassionate and personalized care and support for millions of patients and family members each year.
World-leading academic departments and comprehensive centers of excellence pursue scientific discoveries and transformational educational and clinical advances across the entire spectrum of health and disease.
Aligning with Vanderbilt Health’s Strategic Directions, the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff.
Core Accountabilities:
- Organizational Impact: Delivers job responsibilities that impact own job area/team with some guidance.
- Problem Solving/ Complexity of work: Uses existing procedures, research and analysis to solve standard job related problems that may require some judgement.
- Breadth of Knowledge: Requires subject matter knowledge within a professional area to meet job requirements.
- Team Interaction: Individually contributes to project/ work teams.
Core Capabilities:
Supporting Colleagues:
- Develops Self and Others: Continuously improves own skills by identifying development opportunities.
- Builds and Maintains Relationships: Seeks to understand colleagues priorities, working styles and develops relationships across areas.
- Communicates Effectively: Openly shares information with others and communicates in a clear and courteous manner.
Delivering Excellent Services:
- Serves Others with Compassion: Invests time to understand the problems, needs of others and how to provide excellent service.
- Solves Complex Problems: Seeks to understand issues, solves routine problems, and raises proper concerns to supervisors in a timely manner.
- Offers Meaningful Advice and Support: Listens carefully to understand the issues and provides accurate information and support.
Ensuring High Quality:
- Performs Excellent Work: Checks work quality before delivery and asks relevant questions to meet quality standards.
- Ensures Continuous Improvement: Shows eagerness to learn new knowledge, technologies, tools or systems and displays willingness to go above and beyond.
- Fulfills Safety and Regulatory Requirements: Demonstrates basic knowledge of conditions that affect safety and reports unsafe conditions to the appropriate person or department.
Managing Resources Effectively:
- Demonstrates Accountability: Takes responsibility for completing assigned activities and thinks beyond standard approaches to provide high-quality work/service.
- Stewards Organizational Resources: Displays understanding of how personal actions will impact departmental resources.
- Makes Data Driven Decisions: Uses accurate information and good decision making to consistently achieve results on time and without error.
Fostering Innovation:
- Generates New Ideas: Willingly proposes/accepts ideas or initiatives that will impact day-to-day operations by offering suggestions to enhance them.
- Applies Technology: Absorbs new technology quickly; understands when to utilize the appropriate tools and procedures to ensure proper course of action.
- Adapts to Change: Embraces changes by keeping an open mind to changing plans and incorporates change instructions into own area of work.
Position Qualifications:
Responsibilities:
Certifications:
Work Experience:
Relevant Work Experience
Experience Level:
Less than 1 year
Education:
Associate's
Vanderbilt Health is committed to fostering an environment where everyone has the chance to thrive and is committed to the principles of equal opportunity. EOE/Vets/Disabled.
How to Get Visa Sponsorship as a Clinical Trial Associate
Confirm your degree qualifies for STEM OPT
Clinical Trial Associate roles typically fall under STEM OPT because they require life sciences, biomedical, or public health degrees. Verify your program CIP code with your DSO before applying, since STEM OPT extension eligibility is determined by your specific degree, not the job title.
Target CROs and mid-size biotech companies
Contract research organizations like Covance, ICON, and Parexel hire CTAs at volume and have established OPT and H-1B sponsorship pipelines. Mid-size biotechs often move faster than large pharma and are more willing to sponsor candidates who demonstrate strong attention to regulatory detail.
Highlight any GCP or clinical research coursework
Good Clinical Practice certification and hands-on experience with clinical data, IRB submissions, or trial monitoring are concrete signals to hiring managers. Even coursework or academic research projects involving human subjects or regulated data strengthen your application significantly over candidates without that background.
Frame your OPT timeline clearly in applications
Employers evaluating CTA candidates want to understand your work authorization window upfront. State your OPT start date, STEM extension eligibility, and earliest available start date in your cover letter. Proactively addressing this removes ambiguity and signals maturity in navigating the sponsorship conversation.
Pursue ACRP or SoCRA entry-level certification
The ACRP Associate Clinical Research Professional certification and SoCRA's CCRP credential are recognized by employers hiring at the CTA level. Earning or pursuing one demonstrates commitment to the field and can differentiate you from other OPT candidates who have similar academic backgrounds but no credentials.
Network through clinical research professional associations
Industry associations like ACRP and SoCRA host conferences, webinars, and local chapter events where you can connect directly with CRO and sponsor-side hiring managers. Many CTA openings are filled through referrals before they are posted publicly, making professional community engagement a high-return job search activity.
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Get Access To All JobsFrequently Asked Questions
Do Clinical Trial Associate jobs qualify for STEM OPT?
Most Clinical Trial Associate roles qualify for the 24-month STEM OPT extension if your degree is in a STEM-designated field such as biology, biomedical sciences, public health, or a related life sciences discipline. The eligibility is tied to your degree's CIP code, not the job title itself. Confirm your CIP code with your DSO before relying on STEM OPT eligibility in your job search.
Which types of employers hire OPT students as Clinical Trial Associates?
Contract research organizations are the largest source of CTA hiring and tend to have structured onboarding processes that accommodate OPT work authorization. Pharmaceutical companies, biotechs, and academic medical centers also hire at this level. Browse Clinical Trial Associate jobs on Migrate Mate to filter for employers who actively sponsor or hire OPT students in this field.
Can I work as a Clinical Trial Associate on pre-completion OPT?
Yes, pre-completion OPT allows you to work in a role directly related to your degree field before you graduate. A Clinical Trial Associate role typically qualifies if your degree is in a life sciences or health-related field. You can work part-time during the academic year and full-time during breaks, so confirm those restrictions with your DSO before accepting an offer.
How do I explain OPT work authorization to a clinical research employer?
Be direct and factual. Tell the employer you are authorized to work in the United States on OPT for 12 months, with a potential 24-month STEM extension if your degree qualifies, giving you up to 36 months of work authorization before needing H-1B sponsorship. Most CROs and pharma companies are familiar with OPT and have sponsored international employees before, so this conversation is rarely a dealbreaker.
What should I look for in a Clinical Trial Associate job posting as an OPT student?
Look for postings that mention visa sponsorship, international candidates welcome, or H-1B sponsorship for qualified applicants. Roles listed under a large CRO or established pharmaceutical company are more likely to have sponsorship infrastructure. Avoid roles at very small startups or principal investigator-run sites where the employer may have no prior experience navigating OPT or future sponsorship requirements.
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