Clinical Research Associate Jobs
Clinical Research Associate jobs are open across pharmaceutical, biotechnology, medical device, and contract research organizations, from entry-level coordinators to senior and principal CRAs, with specializations in oncology, cardiovascular, and CNS trials. Find a role that fits from the openings below and apply directly.
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INTRODUCTION
Priovant is committed to developing therapies that address high unmet need in autoimmune disease. Reporting to the Director, Clinical Quality Management, the Clinical Research Associate will collaborate closely with investigative study sites to complete required site visits (SQV, SIV, IMV, COV) and perform site management activities to ensure project timelines and deliverables are met. The CRA must build and maintain strong collaborative relationships with investigative sites, as well as leverage strong knowledge of protocol and regulatory guidelines to ensure protection of subject safety, protocol compliance, adequacy of study staff, and validity of study data. The CRA must be well organized, have high attention to detail skills, adapt quickly to changing priorities, and propose reasonable solutions.
Responsibilities:
- Ensure all activities associated with each type of site visit are completed in compliance with ICH-GCP, SOPs, Clinical Monitoring Plan (CMP), Protocol, Study Plans, Local Laws and Regulations
- Confirm every subject was consented to appropriately and met each eligibility criteria
- Interact with clinical site staff to resolve issues and address findings
- Ensure accurate and timely reporting of AEs, SAEs, and PDs, including any follow-up
- Complete high-caliber, on-time site visit reports and letters for each completed site visit
- Conduct site staff training/retraining
- Assist with site visit report reviews
- Oversee site recruitment and enrollment metrics to ensure project timelines are on target; assist site with recruitment efforts, as requested
- Assist with review of pending queries and action items then propose resolution plans
- Perform thorough IP accountability and reconciliation; oversee IP return/destruction process
- Complete ongoing review of ISF and TMF reconciliation to ensure completeness, accuracy, and inspection readiness of both files
- Assist with clinical quality metrics and PD listing review to identify trends or areas of risk
- Assist in review of SOPs, protocols, informed consent forms, study documents, and study plans
- Perform inspection readiness activities to ensure each site is prepared for potential audits/inspections
- Assist in creation of monitoring tools and training material
- Train other CRAs and team members; may conduct oversight visits to ensure adequacy of CRAs
REQUIREMENTS
- 4-year BA/BS or equivalent degree required, preferably in healthcare or scientific discipline
- Minimum of 4 years of independent monitoring experience; preference is 6+ years with experience at both CRO and Sponsor
- Rare disease or complex study experience
- Deep understanding of ICH, GCP, FDA, and other regulatory guidelines
- Strong knowledge of drug development and clinical research processes
- Familiarity with NDA process and FDA/EMA inspection experience is highly desired
- Experience in Phase II - IV clinical trials preferred
- Risk Based Monitoring, Targeted SDV, and Remote monitoring experience
- Strong technical experience with clinical trial systems (CTMS, EDC, eTMF, ePRO, eREG eSource, EMR, IRT/IXRS, etc.) with the ability to quickly learn new software and technologies
- Dependable with track record of collaborating and making an impact in team settings
- Able to interact professionally and confidently with Principal Investigators and clinical site staff
- Adaptable with strong prioritization skills across multiple projects
- Independent with the professional maturity and foresight to escalate immediately when needed
- Must be willing to travel 70%+
INTRODUCTION
Priovant is committed to developing therapies that address high unmet need in autoimmune disease. Reporting to the Director, Clinical Quality Management, the Clinical Research Associate will collaborate closely with investigative study sites to complete required site visits (SQV, SIV, IMV, COV) and perform site management activities to ensure project timelines and deliverables are met. The CRA must build and maintain strong collaborative relationships with investigative sites, as well as leverage strong knowledge of protocol and regulatory guidelines to ensure protection of subject safety, protocol compliance, adequacy of study staff, and validity of study data. The CRA must be well organized, have high attention to detail skills, adapt quickly to changing priorities, and propose reasonable solutions.
Responsibilities:
- Ensure all activities associated with each type of site visit are completed in compliance with ICH-GCP, SOPs, Clinical Monitoring Plan (CMP), Protocol, Study Plans, Local Laws and Regulations
- Confirm every subject was consented to appropriately and met each eligibility criteria
- Interact with clinical site staff to resolve issues and address findings
- Ensure accurate and timely reporting of AEs, SAEs, and PDs, including any follow-up
- Complete high-caliber, on-time site visit reports and letters for each completed site visit
- Conduct site staff training/retraining
- Assist with site visit report reviews
- Oversee site recruitment and enrollment metrics to ensure project timelines are on target; assist site with recruitment efforts, as requested
- Assist with review of pending queries and action items then propose resolution plans
- Perform thorough IP accountability and reconciliation; oversee IP return/destruction process
- Complete ongoing review of ISF and TMF reconciliation to ensure completeness, accuracy, and inspection readiness of both files
- Assist with clinical quality metrics and PD listing review to identify trends or areas of risk
- Assist in review of SOPs, protocols, informed consent forms, study documents, and study plans
- Perform inspection readiness activities to ensure each site is prepared for potential audits/inspections
- Assist in creation of monitoring tools and training material
- Train other CRAs and team members; may conduct oversight visits to ensure adequacy of CRAs
REQUIREMENTS
- 4-year BA/BS or equivalent degree required, preferably in healthcare or scientific discipline
- Minimum of 4 years of independent monitoring experience; preference is 6+ years with experience at both CRO and Sponsor
- Rare disease or complex study experience
- Deep understanding of ICH, GCP, FDA, and other regulatory guidelines
- Strong knowledge of drug development and clinical research processes
- Familiarity with NDA process and FDA/EMA inspection experience is highly desired
- Experience in Phase II - IV clinical trials preferred
- Risk Based Monitoring, Targeted SDV, and Remote monitoring experience
- Strong technical experience with clinical trial systems (CTMS, EDC, eTMF, ePRO, eREG eSource, EMR, IRT/IXRS, etc.) with the ability to quickly learn new software and technologies
- Dependable with track record of collaborating and making an impact in team settings
- Able to interact professionally and confidently with Principal Investigators and clinical site staff
- Adaptable with strong prioritization skills across multiple projects
- Independent with the professional maturity and foresight to escalate immediately when needed
- Must be willing to travel 70%+
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Find JobsClinical Research Associate Job Market
A snapshot from current openings nationwide, updated as new roles post.
Who's Hiring
- Medpace100
- Rutgers University45
- University of Miami34
- St. Jude Children's Research Hospital28
- Thermo Fisher Scientific25
Top Industries Hiring
- Education546
- Biotechnology & Pharmaceuticals346
- Healthcare & Medical Services333
- Science & Research206
- Consulting & Professional Services72
What Employers Look For
The qualifications that appear most often in clinical research associate jobs.
- Bachelor's degree in life sciences, nursing, or a related clinical field
- ICH E6(R2) Good Clinical Practice certification or equivalent training
- Experience conducting site initiation, interim monitoring, and close-out visits
- Proficiency with electronic data capture systems such as Medidata Rave or Oracle InForm
- Knowledge of FDA regulations, including 21 CFR Parts 11, 50, and 56
- Ability to manage multiple investigative sites concurrently across geographies
Tips for Your Clinical Research Associate Job Search
Tailor your resume to ICH GCP
Hiring managers scan CRA resumes for explicit ICH E6(R2) GCP compliance language. List your GCP certification issuer and the year you completed it. Embed terms like protocol deviation management and site initiation visits so your resume clears automated screening.
Apply early to roles that fit
Migrate Mate lists clinical research associate openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Quantify your site monitoring activity
Replace vague phrases like 'conducted site visits' with specifics: the number of sites you managed concurrently, therapeutic areas covered, and whether visits were on-site, remote, or co-monitoring. Metrics give hiring managers a real picture of your workload capacity.
Target openings by phase and indication
Filter your search by trial phase and therapeutic indication before you apply. A Phase I oncology CRA role demands different experience than a Phase III CNS study. Applying to roles that match your actual monitoring history improves your callback rate significantly.
Prepare deviation scenarios for interviews
CRA interviewers routinely ask how you handled a protocol deviation or a site that missed an enrollment window. Prepare two or three specific examples using the situation, action, and outcome structure. Vague answers about process knowledge rarely advance candidates past the first round.
Negotiate travel expectations before accepting
Travel requirements vary widely across CRA roles, from fully remote data review positions to schedules requiring overnight travel four days a week. Confirm expected travel frequency in writing during the offer stage so both sides have aligned expectations from day one.
Clinical Research Associate Jobs: Frequently Asked Questions
Which companies are hiring the most clinical research associates?
The companies hiring the most clinical research associates right now include Medpace, Rutgers University, and University of Miami, with the largest share of openings in California, Massachusetts, and Texas, based on current listings on Migrate Mate as of June 2026. Contract research organizations and large pharmaceutical sponsors consistently account for the bulk of active postings.
How many clinical research associate jobs are remote?
About 11% of clinical research associate openings are fully remote or hybrid as of June 2026, though the share varies considerably by role type. Remote monitoring positions, which focus on electronic source data verification rather than physical site visits, make up the largest portion of fully remote CRA openings.
How do you become a clinical research associate?
Start with a bachelor's degree in a life sciences field such as biology, pharmacology, or nursing, then complete a GCP certification course to establish your regulatory foundation. Gain exposure to clinical trial operations through a coordinator, data management, or regulatory affairs role. Build site monitoring skills through co-monitoring opportunities alongside experienced CRAs before moving into an independent monitoring position.
Can you get hired as a clinical research associate with no experience?
Entry-level CRA roles exist but are competitive. Employers hiring candidates without direct monitoring experience look for clinical trial coordinator work, research assistant roles at academic medical centers, or internships with contract research organizations. Completing a recognized CRA training program and earning your GCP certificate before applying demonstrates initiative and closes some of the experience gap.
What does the clinical research associate interview process look like?
Most CRA hiring processes include an initial recruiter screen focused on therapeutic background and monitoring experience, followed by a technical interview with a clinical operations lead covering GCP knowledge and protocol deviation handling. A final round often involves a hiring manager or project director and may include a scenario-based question about managing a non-compliant site. Some sponsors also require a writing sample or a brief presentation on a past monitoring visit.
Where can I find and apply to clinical research associate jobs?
You can find and apply to clinical research associate jobs on Migrate Mate, which lists current openings from across the United States in one place. Find roles that match your therapeutic background, monitoring experience, and preferred travel commitment, then apply directly to each listing.
See All 1,426+ Clinical Research Associate Jobs
Jump back to the full list of openings and apply to any clinical research associate role that fits.
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