Consultant / Sr. Consultant – Regulatory Affairs, Pharmacovigilance & Market Research

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 post-marketing 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.