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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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Data Associate I

Labcorp

0 - 1 Years

3.5 – 5.5 LPA

February 2, 2026

Online Application

Product Support Tech Advisor 1 (Junior Data Analyst)

IQVIA

0 - 1 Years

February 2, 2026

Online Application

CDM Programmer II

Thermo Fisher

4+ years

February 1, 2026

Online Application

drug safety systems, EDC programming, and clinical trial payments

Fortrea

2 - 7 Years

February 1, 2026

Online Application

Analyst – Patient Oriented Program (POP)

Novartis

January 31, 2026

Online Application

CRA & Pharmacovigilance

Pharmazone

Freshers - 5 Years

January 30, 2026

Email Application

Centralized Study Specialist II

Fortrea

6–8 years

January 29, 2026

Online Application

Centralized Monitoring Assistant

IQVIA

6 months - 2 Years

January 29, 2026

Online Application

Bioanalytical Team (LCMS)

Navitas Lifesciences

2–6 years

January 28, 2026

Email Application

Pharmacovigilance Associate- Clinical Trial Cases/ LSMV Database skills

ICON

2+ years

January 28, 2026

Online Application

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