Medical Affairs Job at Abbott in Mumbai
Looking to advance your career in a medical affairs job with a global healthcare leader? Abbott is hiring a Manager – Medical Information and Operations in Mumbai. This role offers an excellent opportunity to work at the intersection of clinical research, medical affairs, and regulatory coordination while contributing to impactful healthcare innovations through Abbott careers in India.
Medical Affairs Job Details:
- Job Position: Abbott Manager, Medical Information and Operations
- Location: India > Mumbai: BKC Building
- Category: Medical and Clinical Affairs
About the Company
Abbott is a global healthcare leader committed to helping people live healthier lives through innovative medical devices, diagnostics, pharmaceuticals, and nutrition products. With a strong presence in India, Abbott careers offer professionals the opportunity to work on impactful healthcare solutions while growing in a collaborative and science-driven environment.
Qualifications
- Education Level: Associate Degree
- Experience: Minimum of 1 year of relevant experience in medical affairs or clinical research
Medical Affairs Job Description
This medical affairs job at Abbott involves overseeing medical information and clinical operations activities. The role requires an experienced medical affairs professional who can contribute to clinical trial planning, execution, and reporting while ensuring compliance with regulatory and safety standards. As part of Abbott careers, this position supports the development and post-marketing phases of the company’s products.
Key Responsibilities
- Oversee the direction, planning, and execution of clinical trials and research activities
- Contribute to the implementation of clinical protocols and support completion of final study reports
- Recruit clinical investigators and negotiate study design and associated costs
- Direct human clinical trials, specifically Phase III and Phase IV studies
- Participate in adverse event reporting and safety monitoring responsibilities
- Coordinate and provide reporting information for submissions to regulatory agencies
- Monitor adherence to clinical protocols and determine study completion
- Coordinate and oversee investigator initiations and group studies
- Act as a consultant or liaison with external corporations under licensing agreements when required
