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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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Study Start-Up Submissions Coordinator

Medpace

1 Years+

April 25, 2025

Online Application

Safety Science Analyst

Fortrea

Freshers or 1-2 years

3 - 4.4 LPA

April 25, 2025

Online Application

Consultant

IQVIA

6 Years

April 24, 2025

Online Application

Medical Reviewer

4C Pharma Solutions

2+ years of experience in pharmacovigilance, drug safety, or medical review.

April 24, 2025

Online Application

Oncology Data Specialist (ODS)

Omega Healthcare

0-5 years

April 23, 2025

Online Application

Oncology Data Specialist (ODS)

Omega Healthcare

0-5 years (Freshers can apply)

April 23, 2025

Online Application

Medical Surveillance Specialist 1

IQVIA

2.5 to 6 years

April 23, 2025

Online Application

Pharmacovigilance Associate

ICON

1 - 3 Years

4 - 7 LPA

April 22, 2025

Online Application

Safety Science Analyst

Fortrea

0 - 1 Year

April 22, 2025

Online Application

Medical Science Liaison – Plasma Derived Therapies (PDT)

Takeda

2-3 years

April 22, 2025

Online Application

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