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Abbott, a global leader in healthcare and medical research, is seeking a Pharmacovigilance (PV) Specialist in Mumbai. This role is ideal for experienced professionals in Medical Affairs looking to apply their expertise in clinical trials, adverse event reporting, and regulatory compliance. If you are passionate about advancing patient safety and contributing to innovative healthcare solutions, this opportunity is perfect for you.
Key Responsibilities
As a PV Specialist at Abbott, you will:
- Oversee planning, execution, and data collection activities of clinical trials (Phase III & IV).
- Implement clinical protocols and facilitate completion of final reports.
- Recruit clinical investigators and negotiate study design, timelines, and costs.
- Direct human clinical trials for company products under development.
- Participate in adverse event reporting and monitor safety responsibilities.
- Coordinate submission reports to regulatory agencies and ensure adherence to protocols.
- Oversee investigator initiations and group studies.
- Serve as a consultant/liaison with other corporations for licensing agreements when required.
Required Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or Medical Affairs.
- Proven experience in pharmacovigilance, clinical trials, or medical affairs roles.
- Strong knowledge of regulatory requirements and safety monitoring.
- Excellent communication, negotiation, and project management skills.
- Ability to work independently under limited supervision.
Benefits
- Competitive salary package (INR 12–18 LPA, depending on experience).
- Opportunity to work with a leading global healthcare organization.
- Exposure to innovative clinical research and regulatory practices.
- Professional growth in Medical Affairs and Pharmacovigilance.
- Collaborative and dynamic work environment.
How to Apply
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