Advertisement
If you are an experienced clinical research professional looking to step into a leadership-driven role, this Senior Clinical Research Supervisor job in Mumbai offers a strong opportunity to work with a global MedTech leader. At Medtronic, you will drive clinical trials, regulatory strategy, and team performance while contributing to innovative healthcare solutions.
This role combines clinical operations, regulatory affairs, and people management, making it ideal for professionals aiming to transition into strategic clinical leadership roles.
📌 Job Overview
- Job Title: Senior Clinical Research Supervisor
- Location: Mumbai, Maharashtra, India (Remote flexibility)
- Job Type: Full-time
- Department: Clinical Research / Regulatory Affairs
- Experience: 3–8+ years (with leadership exposure)
- Industry: Medical Devices / Clinical Research
🧪 Key Responsibilities
Clinical Research & Trial Leadership
- Lead execution of local and global clinical studies ensuring scientific validity and ethical compliance
- Oversee clinical trial operations, including planning, monitoring, and delivery timelines
- Ensure accurate evaluation of safety and efficacy data
Regulatory Strategy & Submissions
- Develop and implement global regulatory strategies for product approvals
- Prepare and review regulatory submissions in compliance with international guidelines
- Coordinate with regulatory authorities and ensure timely approvals
Stakeholder Management
- Represent Medtronic in the region for clinical research activities
- Build relationships with internal teams, investigators, and regulatory bodies
- Gather and incorporate feedback from local stakeholders
Team Leadership & People Management
- Manage and mentor a team of clinical professionals
- Conduct performance reviews, coaching, and development planning
- Drive team alignment with organizational goals and clinical milestones
Operational Excellence
- Ensure adherence to SOPs, GCP, and regulatory standards
- Improve clinical processes, systems, and workflows
- Support budget planning and resource allocation
🎓 Qualifications & Skills
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field
- 3+ years of relevant experience (or 1+ year with advanced degree)
- Strong knowledge of:
- Clinical trial processes (Phase I–IV)
- Regulatory frameworks (FDA, EMA, CDSCO)
- GCP and ICH guidelines
- Proven team leadership and project management skills
- Excellent communication and stakeholder management abilities
💼 Benefits & Compensation
- Competitive salary with performance incentives (MIP bonus plan)
- Flexible work environment (remote options available)
- Career growth in a global MedTech leader
- Learning & development programs
- Comprehensive employee benefits and wellness support
💰 Salary Insight (India Benchmark)
- Estimated Salary Range: ₹18,00,000 – ₹28,00,000 per annum
(Based on experience, leadership scope, and industry standards)
🚀 Why This Role is High-Value
This clinical research supervisor role is highly strategic because it integrates:
- Clinical trial leadership
- Regulatory affairs exposure
- People management
- Cross-functional collaboration
It is a strong pathway toward roles like:
- Clinical Operations Manager
- Regulatory Affairs Manager
- Clinical Program Director
📥 How to Apply
Advertisement