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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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ICON PLc

1 - 3 Years

August 11, 2025

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Analyst

IQVIA

1-3 years

August 11, 2025

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PharmaQuant

0 - 2 Years

August 10, 2025

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Certara

1-2 years

August 9, 2025

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ICON

0 - 1 Years

August 8, 2025

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Pharmacovigilance Services Associate

Accenture

0 - 2 Years

3 - 4 LPA

August 8, 2025

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Real World Evidence Analyst II

Fortrea

1 - 3 Years

August 7, 2025

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Pharmacovigilance MICC and Quality Control – Pharmacovigilance Literature

AnaCipher

1 - 7 Years

August 7, 2025

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Quality Assurance Auditor II

ICON

2 years

August 7, 2025

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Pharmacovigilance Specialist

Medifodil

3+ years

August 7, 2025

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