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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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Bioinformatics Biostatistics Data Science & Analytics Clinical SAS Programming HEOR & Real-World Evidence Medical Writing Scientific Writing Medical Science Liaison

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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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Analyst Job at (| Full-Time)

Clinovis Technologies

0 - 2 Years

September 25, 2025

Email Application

Safety Aggregate Report Specialist & Manager

IQVIA

3 -6 Years

September 24, 2025

Online Application

Regulatory Affairs Associate & Consultant

Parexel

4 - 10 Years

September 24, 2025

Online Application

Medical Imaging Read Services Specialist

Clario

0 - 1 Years

4 - 7 LPA

September 24, 2025

Online Application

Associate Project Support

IQVIA

1–2 years in clinical research

September 24, 2025

Online Application

Pharmacovigilance Reporting Associate

ICON

1 - 3 Years

September 23, 2025

Online Application

Assistant I PSS

Fortrea

0 - 1 Years

September 23, 2025

Online Application

Medical Safety Advisor

IQVIA

3 years

September 23, 2025

Online Application

Senior Medical Writer (Disclosure)

Syneos Health

4 years +

September 23, 2025

Email Application

Pharmacovigilance Interns and Pharmacovigilance Team Leads/SMEs/Associate Managers

CliniResource

0 - 5 Years

September 23, 2025

Email Application

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