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Clinical Research Supervisor

Medtronic
Medtronic
1-3 years
Not Disclosed
10 Dec. 15, 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

Location: Mumbai, Maharashtra, India
Work Type: Full-Time | Remote
Job Requisition ID: R54470
Experience Required: Minimum 1–3 Years (Clinical Research / Regulatory / Medical Devices)
Industry: Medical Devices | Clinical Research | Regulatory Affairs


About Medtronic

Medtronic is a global leader in healthcare technology, dedicated to improving access, equity, and outcomes in healthcare worldwide. With a mission to alleviate pain, restore health, and extend life, Medtronic empowers professionals to innovate with purpose and make a meaningful impact across the global healthcare ecosystem.


Position Overview

Medtronic is seeking a Clinical Research Supervisor to provide leadership and operational oversight for clinical studies and associated regulatory activities. This role is responsible for ensuring clinical trials are scientifically sound, ethically conducted, and compliant with global regulatory requirements. The position involves supervising clinical research teams, managing both local and global studies, and contributing to timely product approvals across Medtronic’s therapy areas.


Key Responsibilities

  • Lead and oversee the execution of clinical studies to ensure scientific validity, ethical conduct, and regulatory compliance.

  • Provide leadership for regulatory affairs activities supporting product development and approval.

  • Develop and implement regulatory strategies to achieve timely approvals from global health authorities.

  • Ensure accuracy, quality, and compliance of regulatory submissions in line with applicable guidelines and approvals.

  • Manage and execute local and global clinical research projects across multiple Medtronic therapy areas.

  • Represent Medtronic from a clinical research perspective within the assigned country or region.

  • Build and maintain strong relationships with internal stakeholders, investigators, regulatory authorities, and external partners.

  • Collect and relay feedback from local customers, investigators, and regulatory bodies to internal teams.

  • Supervise, mentor, and develop clinical research team members, ensuring alignment with departmental goals and performance standards.

  • Plan operational objectives, manage team workflows, allocate resources, and monitor project timelines and deliverables.

  • Support continuous improvement initiatives by enhancing clinical research processes and operational systems.


People Management Responsibilities

  • Provide direct supervision and day-to-day guidance to clinical research and support staff.

  • Conduct performance reviews, one-on-one meetings, coaching, and development planning for direct reports.

  • Contribute to hiring, promotion, performance evaluation, and reward decisions for team members.

  • Foster a collaborative, inclusive, and performance-driven team environment.


Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, Biomedical Sciences, or a related discipline.

  • Minimum 1 year of relevant experience in clinical research, regulatory affairs, medical devices, or related operational roles.

  • Demonstrated understanding of clinical trial conduct, regulatory requirements, and ethical guidelines.

  • Prior experience in team supervision or project coordination is preferred.


Required Skills and Competencies

  • Strong knowledge of clinical research operations and regulatory compliance.

  • Working understanding of global regulatory submission processes.

  • Effective leadership, coaching, and team management skills.

  • Strong communication and stakeholder engagement abilities.

  • Ability to manage multiple studies and priorities in a remote working environment.

  • Problem-solving mindset with the ability to recommend process and system improvements.


Work Environment & Benefits

  • Remote work flexibility with collaboration across regional and global teams.

  • Competitive salary and comprehensive benefits package.

  • Eligibility for Medtronic’s short-term incentive program (Medtronic Incentive Plan – MIP).

  • Access to learning resources, leadership development programs, and long-term career growth opportunities.


Why Join Medtronic

At Medtronic, you will be part of a mission-driven organization that combines engineering excellence with clinical innovation. This role offers the opportunity to lead impactful clinical research initiatives while developing people, processes, and products that transform patient lives globally.


Equal Opportunity Employer

Medtronic is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, religion, gender, age, disability, sexual orientation, gender identity, or any other legally protected status.