At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
Responsibilities may include the following and other duties may be assigned.
- Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval.
- Studies must be scientifically valid, meet all relevant regulatory requirements and be conducted within ethical guidelines.
- The end result of the clinical studies must be a fair assessment of the safety and efficacy of the tested product (s) and attainment of product approvals in a timely matter.
- Develops and implements regulatory strategies to obtain timely product approvals form worldwide regulatory bodies.
- Ensures regulatory submissions are accurately prepared and comply with regulatory approvals.
- People working within region/country may also have the responsibilities that include:
- Represents Medtronic from a clinical research respective within the country / region and also collects feedback from local customers and authorities.
- Builds and maintains a solid network and close relationship with the various internal and external parties.
- Leads execution for both local and global studies, manages clinical research projects over all of the Medtronic therapies across multiple businesses.
PEOPLE MANAGEMENT FUNCTIONAL CAREER STREAM: Management and supervisory professionals with one or more employees who are focused on tactical, operational and some strategic activities within a specified area. Levels within the management career stream typically have six or more direct reports. The majority of time is spent overseeing their area of responsibility, managing performance, developing talent, engagement and inclusion, communicating business and operational developments, plannin
📌 Clinical Research Supervisor (Mumbai)
🏢 Medtronic
📍 Mumbai
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