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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 & Safety

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

Manufacturing & Quality

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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Senior Medical Reviewer GCH

Lilly

Minimum 2 Years

August 13, 2026

Online Application

Pharmacovigilance

Cognizant

1 - 4 Years

August 13, 2026

Online Application

Data Management & Clinical Research Centralized Study Associate

Labcorp

0 - 1 Years

August 13, 2026

Online Application

Study Support Assistant

ICON

1+ years in clinical research and related activities

August 13, 2026

Online Application

Area Medical Advisor, Vaccines

Pfizer

0–2 Years

August 13, 2026

Online Application

Centralized Monitoring Assistant

IQVIA

6 months - 2 Years

August 12, 2026

Online Application

Contract Specialist

Parexel

2 Years+

August 12, 2026

Online Application

Medical Science Liaison

BMS

1–2 years of Field Medical experience

August 12, 2026

Online Application

Regulatory Affairs Associate

Parexel

3+ years

August 11, 2026

Online Application

ICSR Case Processing SPE/SME

2COMS

Life Sciences / Pharmacy / Medical Sciences or Equivalent

August 11, 2026

Online Application

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