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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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Clin Resourcing and Operations Analyst

IQVIA

0-2 years

February 18, 2025

Online Application

Safety Science Coordinator and QA Controlled Docs Coordinator

Fortrea

1 - 3 Years

4 - 6 Lacs per anum

February 18, 2025

Online Application

Safety Science Specialist

Fortrea

3-4 years

February 17, 2025

Online Application

Safety Writer and Safety Writing Assistant II

Fortrea

6 Months - 4 Years

February 17, 2025

Online Application

Pharmacovigilance Trainer

Vizen Life Sciences

4 - 8 Years

February 17, 2025

Online Application

Biostatistician (referral)

IQVIA

1 - 3 Years

February 15, 2025

Online Application

Regulatory Affairs Specialist

Thermo Fisher Scientific

4 - 6 Years

February 13, 2025

Online Application

Case Processing / Aggregate Report Writer in PV

Veeda Lifesciences

4 - 6 Years

7 - 10 LPA

February 12, 2025

Online Application

Trial Master File Specialist (TMF) & Site Network Specialist (Global Feasibility)

Biorasi

1 - 5 Years

February 10, 2025

Online Application

Principal Statistical Programmer

ICON plc

3 - 5 Years

February 10, 2025

Online Application

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