{"@context":"https://schema.org","@type":"JobPosting","title":"Freelance Consultant - Regulatory Affairs, Pharmacovigilance & Market","description":"

Roles & Responsibilities

Consultant / Sr. Consultant Regulatory Affairs, Pharmacovigilance & Market

Research

Handle regulatory affairs activities (70%) including submissions,

registrations, renewals, and lifecycle management.

Prepare and review regulatory dossiers, documentation, and compliance

records.

Coordinate with CDSCO and regulatory authorities for approvals and

compliance.

Track regulatory updates and manage timelines, trackers, and records.
Support pharmacovigilance activities such as safety reporting and postmarketing

compliance.

Conduct primary market research (30%), including stakeholder interviews and

insight generation.

Collaborate with cross-functional teams to deliver timely and high-quality

outputs.

Requirements:

Degree in Pharmacy/Life Sciences; 5–8 years of relevant experience.

Strong knowledge of regulatory frameworks, PV, and primary research

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