Clinical Research Associate Jobs in North Carolina
Clinical Research Associate jobs in North Carolina are open across Durham, Chapel Hill, and Burlington and other North Carolina metros, with employers like Atrium Health, Cambridge Pharma Consulting, and Duke University hiring at every experience level. Find a role that fits below and apply directly.
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Showing 5 of 39+ Clinical Research Associate jobs
INTRODUCTION
Remote Sr. CRA position in the oncology space! This Jobot Job is hosted by: Audrey Block. Are you a fit? Easy Apply now by clicking the "Easy Apply" button and sending us your resume.
SALARY
Salary: $120,000 - $140,000 per year
About us
Prep-Ipo Biotech company with strong funding, focused in the Oncology space. We are looking for 1-2 Senior CRA's to join our team!
WHY JOIN US?
- Opportunity to wear different hats in a small company - lots of growth!
- Strong pipeline
- Good benefits and compensation package
- 401k with a match
- Flexible schedule
JOB DETAILS
Looking for 1-2 Senior CRAs to join the team! Oncology experience is REQUIRED. Please note - this position requires domestic travel about 30-40% of the time!
- Develops strong investigative site relationships and ensures continuity of investigative site relationships through all phases of the trial
- Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations
- Performs remote and on-site monitoring & oversight activities using various tools to ensure data generated at the site are complete, accurate, and unbiased; subjects' rights, safety, and well-being are protected
- Collects, reviews, and monitors required regulatory documents for study start-up, study maintenance, and study close-out
- Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, missing data and data queries, protocol deviations, regulatory documentation, site audits/inspections, and overall site performance
- Identifies, assesses, and resolves site performance, quality, or compliance problems and escalates per protocol to upper management
- Works with in-house Clinical Trial Assistant to collect, review, and monitor required regulatory documentation for study start-up, study maintenance, and study close-out
- Manages and maintains information and documentation in Clinical Trial Management System, electronic Trial Master File, and various other systems as appropriate and per timelines
Interested in hearing more? Easy Apply now by clicking the "Easy Apply" button.
Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy.
Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page!
INTRODUCTION
Remote Sr. CRA position in the oncology space! This Jobot Job is hosted by: Audrey Block. Are you a fit? Easy Apply now by clicking the "Easy Apply" button and sending us your resume.
SALARY
Salary: $120,000 - $140,000 per year
About us
Prep-Ipo Biotech company with strong funding, focused in the Oncology space. We are looking for 1-2 Senior CRA's to join our team!
WHY JOIN US?
- Opportunity to wear different hats in a small company - lots of growth!
- Strong pipeline
- Good benefits and compensation package
- 401k with a match
- Flexible schedule
JOB DETAILS
Looking for 1-2 Senior CRAs to join the team! Oncology experience is REQUIRED. Please note - this position requires domestic travel about 30-40% of the time!
- Develops strong investigative site relationships and ensures continuity of investigative site relationships through all phases of the trial
- Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations
- Performs remote and on-site monitoring & oversight activities using various tools to ensure data generated at the site are complete, accurate, and unbiased; subjects' rights, safety, and well-being are protected
- Collects, reviews, and monitors required regulatory documents for study start-up, study maintenance, and study close-out
- Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, missing data and data queries, protocol deviations, regulatory documentation, site audits/inspections, and overall site performance
- Identifies, assesses, and resolves site performance, quality, or compliance problems and escalates per protocol to upper management
- Works with in-house Clinical Trial Assistant to collect, review, and monitor required regulatory documentation for study start-up, study maintenance, and study close-out
- Manages and maintains information and documentation in Clinical Trial Management System, electronic Trial Master File, and various other systems as appropriate and per timelines
Interested in hearing more? Easy Apply now by clicking the "Easy Apply" button.
Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy.
Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page!
See All 39 Clinical Research Associate Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find JobsClinical Research Associate Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
Clinical Research Associate Job Market in North Carolina
A snapshot from current North Carolina openings, updated as new roles post.
Who's Hiring
- Atrium Health6
- Cambridge Pharma Consulting6
- Duke University5
- University of North Carolina at Chapel Hill4
- Asklepios Biopharmaceutical3
Top Industries Hiring
- Healthcare & Medical Services14
- Biotechnology & Pharmaceuticals13
- Education10
- Consulting & Professional Services3
- Science & Research3
What North Carolina Employers Look For
The qualifications that appear most often in clinical research associate jobs across North Carolina.
- 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
Clinical Research Associate Jobs in North Carolina: Frequently Asked Questions
How many clinical research associate jobs are there in North Carolina?
There are 39+ clinical research associate openings in North Carolina on Migrate Mate as of June 2026, with the most roles in Durham, Chapel Hill, and Burlington. New positions post regularly as employers across North Carolina hire.
Which North Carolina cities have the most clinical research associate jobs?
Durham, Chapel Hill, and Burlington have the most clinical research associate openings in North Carolina right now, with additional roles spread across smaller metros statewide.
Which companies hire clinical research associates in North Carolina?
Employers hiring clinical research associates in North Carolina include Atrium Health, Cambridge Pharma Consulting, and Duke University, based on current listings on Migrate Mate as of June 2026.
Are there remote clinical research associate jobs in North Carolina?
Yes. About 15% of clinical research associate openings tied to North Carolina are remote or hybrid as of June 2026. The rest are on-site roles based in North Carolina metros.
How do I apply for clinical research associate jobs in North Carolina?
You can apply to clinical research associate jobs in North Carolina directly on Migrate Mate. Search the listings above, find roles that match your experience and preferred North Carolina location, then apply to each one that fits.
See All 39 Clinical Research Associate Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
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