This role has closed. ProTrials has taken the posting down.
hirly last saw it live on 1 October 2026. See similar open roles below, or browse the live board.
ProTrials
Senior Clinical Research Associate
Regional
Similar open jobs
- Senior Clinical Research Associate - Metabolic - CentralWorldwide · 2 LocationsFirst seen today
- Senior Clinical Research Associate - Oncology - Midwest/CentralWorldwide · 2 LocationsFirst seen today
- Clinical Research Associate IUtaustin · AUSTIN, TXFirst seen today
- Social Science/Humanities Research Associate III - Texas Center for Disability StudiesUtaustin · PICKLE RESEARCH CAMPUSFirst seen today
- Equity Research Associate, Healthcare SectorWellington · Boston, MA, United StatesFirst seen today
- Equity Research Associate - Industrials SectorWellington · Boston, MA, United StatesFirst seen today
- Physician-GastroenterologyWvumedicine · Berkeley Medical Center (BMC)First seen today
- Physician - Interventional Cardiology (UTN)Wvumedicine · Uniontown Hospital (UNTWN)First seen today
hirly's read of this role
- Role family
- Healthcare
- Seniority
- Senior
- Stated salary
- $130,000 – $155,000 per year
- Country
- US
- Work mode
- Remote-friendly
- First seen by hirly
- 11 Sept 2026
Derived automatically from the posting.
the posting
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries.
Our people are the heart of everything we do. We believe great work happens when team members feel valued, supported, and empowered. At ProTrials, you’ll join a collaborative community committed to making a meaningful impact on global health.
We are excited to connect with skilled individuals who share our passion for advancing clinical research with care, integrity, and excellence.
ABOUT THE JOB
The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. Responsibilities of a Sr. CRA include ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. Sr. CRAs may be required to travel up to 65%.