Associate – Regulatory Affairs
CLINCHOICE
Advertisement
Job Description
 Location: Mumbai, India
Department: Medical and Clinical Affairs
Job Overview
 As a Medical Advisor, you will be an experienced individual contributor in the Medical Affairs function, applying specialized knowledge to support the design, oversight, and execution of clinical trials and medical research activities. Working under limited supervision, you will play a key role in ensuring that company products are developed, tested, and monitored according to regulatory and scientific standards.
Role & Responsibilities
- Oversee the planning, direction, and execution of clinical trials and research activities.
- Contribute to the implementation of clinical protocols and facilitate the completion of final study reports.
- Recruit and engage clinical investigators, negotiating study design and associated costs.
- Direct Phase III and IV clinical trials for company products under development.
- Participate in adverse event reporting and safety monitoring activities.
- Coordinate and prepare regulatory submissions and reports for relevant health authorities.
- Monitor protocol adherence and determine study completion milestones.
Educational Qualification
- Advanced degree in Medicine, Pharmacy, Life Sciences, or a related field.
- Proven experience in Medical Affairs and clinical research management.
- Strong understanding of clinical development processes and regulatory requirements.
- Excellent communication, analytical, and organizational skills.
- Ability to work independently while collaborating effectively with cross-functional teams
Location
 Mumbai, India
Advertisement
Recent Jobs
Clinical Research Coordinator
MS Clinical Research
Safety Science Coordinator I
Fortrea
R&D Operations – Analyst 1
Johnson&Johnson
Medical Advisor
Abbott