Clinical Research Associate

External job listingat Infoservllc

Requirements 2+ years of independent Clinical Site Monitoring experience Hands-on experience with SIVs, IMVs, and COVs Strong knowledge of ICH-GCP guidelines and FDA regulations Experienc...

External source - not verified2 weeks agoOpen until: Jan 10, 2027

Salary

Not provided

Location

Boston, United States

Employment type

Full time

Workplace

Not provided

Clinical Research Associate

Boston, United States

Job description

Requirements

2+ years of independent Clinical Site Monitoring experience
Hands-on experience with SIVs, IMVs, and COVs
Strong knowledge of ICH-GCP guidelines and FDA regulations
Experience with Source Data Verification (SDV) and Source Data Review (SDR)
Clinical monitoring reports, protocol deviation management, and site documentation
Bachelor's degree in Life Sciences, Nursing, or a related discipline
Preferred: 3–5+ years of CRA experience in Pharma, Biotech, or CRO environments
Preferred: Phase I–IV clinical trial experience
Preferred: Familiarity with RBM, eTMF, CTMS, and EDC systems

Schedule

Regional clinical site travel required.

How to apply

Comment “INTERESTED”, email your resume, or message me directly on LinkedIn.

Location

Boston, MA
Tampa, FL
Chicago, IL
Southern California
USA Remote
Candidates must live within approximately 1 hour of the assigned onsite office/region.