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Clinical Research Clinical Data Management (CDM)Pharmacovigilance Medical Writing Trial Master File (TMF)Medical Coding SAS Data Sciences Medical Science Liaison (MSL)Medical Reviewer RWE / HEOR

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Clinical Research Clinical Data Management Pharmacovigilance Trial Master File (TMF)Regulatory Affairs Medical Reviewer Medical Coding Pharmacist Medical Devices

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Safety & PV Specialist | ICSR case processing, PMS activities, and spontaneous reporting

Syneos Health

1 - 8 Years

May 18, 2026

Online Application

Safety Systems Associate II & Programmer Analyst I

Fortrea

2 - 7 Years

May 18, 2026

Online Application

Data Quality Analyst & Senior Global Regulatory Scientist

ICON

3 Years+

May 18, 2026

Online Application

Program/Project Coordinator – Clinical Research Coordinator Role

ICON

Prior experience in project coordination, administration, or clinical research preferred

May 18, 2026

Online Application

Associate Specialist Strategic Forecasting

Merck

0–3 years

May 15, 2026

Online Application

Global Project Specialist I & II

Imaging Endpoints

2 - 3 Years+

May 15, 2026

Online Application

Senior Drug Safety Associate

Soterius

2–4 Years

May 15, 2026

Online Application

TMF Classifier I, Central Monitor Assistant

Fortrea

0 - 3 Years

May 15, 2026

Online Application

Associate Study Coordinators

Labcorp

0–2 years

May 15, 2026

Online Application

Randomization & Study Product Coordinator, Clinical Data Coder, eClinical Coordinator, Data Coordinator, and Experienced Clinical Database Programmer

Medpace

0 - 5 Years+

May 15, 2026

Online Application

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