Clinical Research Supervisor

Medtronic

1+ years

Not Disclosed

Mumbai

10 Dec. 12, 2025

Job Description

Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Supervisor – Medtronic (Remote, Mumbai, India)

Job ID: R54470
Location: Remote (Mumbai, Maharashtra, India)
Employment Type: Full-time

About Medtronic

Medtronic is a global leader in healthcare technology, advancing innovative solutions that alleviate pain, restore health, and improve lives. With a diverse workforce of over 95,000 professionals and a mission-driven culture, Medtronic focuses on transforming patient outcomes through science, engineering, and compassionate care. The company offers opportunities to drive clinical excellence while contributing to healthcare access and equity worldwide.

Position Overview

The Clinical Research Supervisor will provide leadership in the execution of clinical studies and ensure compliance with global regulatory standards. This role is responsible for overseeing clinical research operations, managing study teams, maintaining stakeholder relationships, and supporting product approval processes. The position requires strong people management skills, regulatory knowledge, and the ability to manage multiple studies across different therapies.

Key Responsibilities

Lead the planning, conduct, and oversight of clinical studies, ensuring scientific validity and adherence to regulatory and ethical guidelines.
Support regulatory affairs activities related to product approvals across global markets.
Ensure regulatory submissions and study documentation meet accuracy and compliance standards.
Represent Medtronic in clinical research discussions with regional authorities and local stakeholders.
Build strong relationships with internal teams, external partners, investigators, and regulatory bodies.
Manage execution of local and global studies across multiple therapeutic areas.
Supervise clinical research teams, providing direction, workload oversight, and performance management.
Guide team members through coaching, mentoring, and development initiatives.
Ensure departmental goals, productivity standards, and project timelines are met.
Contribute to improvements in clinical processes, systems, and operational efficiency.

Leadership Responsibilities

Oversee a team of support professionals, including technicians, production staff, and clerical contributors.
Provide input on hiring, promotions, performance reviews, and rewards.
Maintain workflow continuity, resource allocation, and productivity.
Communicate operational updates, priorities, and expectations clearly and effectively.

Role Expectations and Decision-Making

Operate with moderate autonomy, performing individual tasks alongside supervisory duties.
Plan operational objectives and manage schedules for team members.
Address defined operational challenges and recommend process enhancements.
Communicate effectively with internal teams, vendors, customers, and external stakeholders.

Required Qualifications & Experience

Education: Bachelor’s degree (or equivalent qualification meeting 8 C.F.R. § 214.2(h)(4)(iii)(A)).
Experience: Minimum 1 year of relevant clinical research or operational experience.
Understanding of basic management principles including work scheduling, coaching, and process oversight.
Broad technical or operational knowledge within clinical research or associated disciplines.
Strong communication skills and the ability to collaborate across cross-functional teams.

Physical Requirements

Responsibilities may require certain physical tasks consistent with clinical and operational environments. Specific requirements will be discussed during the hiring process.

Benefits & Compensation

Medtronic offers competitive compensation and a comprehensive benefits package tailored to support employees at every stage of their career. This position is eligible for the Medtronic Incentive Plan (MIP), a performance-based short-term incentive.

Why Join Medtronic?

Medtronic fosters a culture rooted in innovation, integrity, and inclusion. Employees contribute to high-impact work across engineering, R&D, clinical operations, and global healthcare strategy. By joining the organization, you become part of a mission-driven team focused on engineering meaningful solutions that make a real difference in patients’ lives.

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Clinical Research Supervisor

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