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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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Quality Assurance (QA)Quality Control (QC)Pharmaceutical Production R&D & Formulation Pharmaceutical Microbiology Pharmaceutical Packaging Pharmaceutical Warehouse Pharmaceutical Engineering Environmental Health & Safety Effluent Treatment Plant (ETP)Technology Transfer (TDS)

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Research Associate

Clarivate

0 - 1 Years

3 - 4 LPA

April 16, 2025

Online Application

Clinical Data Specialist & Safety System Coordinator

Fortrea

1 - 5 Years

4.5 - 11 LPA

April 16, 2025

Online Application

Clinical Data Management Associate

Veeda Lifesciences

3-5 Years

April 16, 2025

Email Application

Clinical Process Associate

IQVIA

2 Years

April 16, 2025

Online Application

Clinical Programmer (EDC)

Atorus

1 to 5 Years

April 15, 2025

Online Application

Research Associate II (Research and Development)

Vantive

April 13, 2025

Online Application

Site Readiness and Regulatory Specialist I

Fortrea

regulatory affairs, clinical research, or site readiness is a plus (1 Years +)

30K - 40K Per Month

April 12, 2025

Online Application

STEM Content Analyst

Clarivate

2+ years

5 - 8 LPA

April 11, 2025

Online Application

Pharmacovigilance, Clinical Validation & Study Start-Up Roles

ICON plc

1 - 5 Years

4 - 12 LPA

April 11, 2025

Online Application

Clinical Data Analyst

Fortrea

1 - 2 Years

3.5 - 5 LPA

April 11, 2025

Online Application

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