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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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Graduate Pharmacovigilance Associate

ICON plc

Freshers

December 15, 2025

Online Application

Freshers Opening

SpinoS Lifescience

Fresher

December 15, 2025

Email Application

Regulatory Medical Writer

JSS Medical Research

2–6 years

December 13, 2025

Email Application

Associate Medical Writer

IQVIA

1 Years+

December 12, 2025

Online Application

Statistical Programmer

Sylphid Analytics

0–7 Yrs

December 12, 2025

Email Application

Senior Site Activation Coordinator

IQVIA

2 years

December 11, 2025

Online Application

Centralized Site Associate

IQVIA

1 - 4 Years

December 11, 2025

Email Application

Senior Safety Reporting Specialist

Thermo Fisher Scientific

3+ years

December 11, 2025

Online Application

eCOA Screen Review & Data Quality Analyst

ICON Plc

2 years+

December 9, 2025

Online Application

Business Process Specialist

Clario

2 years

December 9, 2025

Online Application

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