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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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Medical review, Centralized monitoring, Statistical monitoring, Functional Programmer

Novo Nordisk

0 - 11 Years

January 2, 2026

Online Application

Senior Associate – CMC Regulatory Affairs

ClinChoice

January 2, 2026

Online Application

Sr. CDM Programmer (EDC)

Thermo Fisher scientific

5+ Yrs

January 2, 2026

Online Application

Safety Science Coordinator I

Fortrea

0 - 1 Years

29K Per Month

January 2, 2026

Online Application

Sample Management Specialist

Precision For Medicine

2–3 years

January 2, 2026

Online Application

Associate Statistical Monitor

Novo Nordisk GBS

0 - 2 Years

January 1, 2026

Online Application

Pharmacovigilance Assessor

TCS

2–3 years

January 1, 2026

Online Application

Project Specialist – Operations

Signant Health

1 - 5 Years

December 31, 2025

Online Application

Analyst, Project Support Specialist, and Senior Global Data Associate

IQVIA

1 Years+

December 31, 2025

Online Application

Pharmacovigilance ICSR Safety Case Processing

Horizontal (IQVIA) Contract Role

Fresher

December 31, 2025

Email Application

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