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Clinical Research Supervisor

Medtronic
Medtronic
1+ years
Not Disclosed
10 Jan. 1, 2026
Job Description
Job Type: Full Time 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 – Remote

Company: Medtronic
Location: Mumbai, Maharashtra, India (Remote)
Employment Type: Full-Time, Permanent
Job ID: R54470
Posted: 22 Days Ago
Category: Clinical Research / People Management


About Medtronic

Medtronic is a global leader in healthcare technology, dedicated to addressing the world’s most challenging health problems. With over 95,000 employees across the globe, Medtronic combines engineering, innovation, and a commitment to improving lives to develop solutions that alleviate pain, restore health, and extend life.

At Medtronic, employees thrive in an environment that values exploration, collaboration, and inclusion while driving breakthroughs that impact patients worldwide.


Role Overview

The Clinical Research Supervisor will provide leadership for the conduct of clinical studies, ensuring regulatory compliance, scientific validity, and ethical integrity. This role oversees clinical research projects, manages teams, and contributes to regulatory strategy to achieve timely product approvals. The position also involves talent management, operational planning, and direct supervision of staff within clinical research functions.

This role is suitable for candidates with a combination of clinical research expertise, leadership skills, and experience in managing teams in a regulated environment.


Key Responsibilities

Clinical Research Oversight

  • Lead execution of local and global clinical studies across multiple Medtronic therapy areas

  • Ensure clinical studies meet scientific, ethical, and regulatory requirements

  • Develop and implement regulatory strategies to obtain timely approvals from international regulatory authorities

  • Ensure accuracy and compliance of regulatory submissions

People Management & Leadership

  • Supervise a team of clinical research staff, providing tactical and technical guidance

  • Mentor, coach, and develop team members to meet performance objectives

  • Conduct performance reviews, 1:1s, and guide staff development initiatives

  • Allocate resources, manage workflows, and ensure operational efficiency

Stakeholder Collaboration & Communication

  • Represent Medtronic in clinical research matters within the region/country

  • Build and maintain strong relationships with internal teams, external vendors, and regulatory authorities

  • Share information and solutions effectively to support project goals

Operational & Process Management

  • Plan and oversee operational objectives for the team

  • Monitor schedules, resource allocation, and daily department activities

  • Recommend enhancements to processes, systems, and workflows to improve efficiency


Required Qualifications & Experience

  • Education: Bachelor’s degree in Life Sciences, Pharmacy, or related field (equivalent qualifications recognized internationally)

  • Experience: Minimum 1 year of relevant clinical research or operational experience (management experience preferred)

  • Broad knowledge of technical and operational practices within clinical research

  • Understanding of regulatory requirements, GCP, and ethical guidelines for clinical studies

  • Strong leadership, coaching, and people management skills


Skills & Competencies

  • Ability to plan, prioritize, and manage team performance effectively

  • Excellent communication and stakeholder management skills

  • Analytical thinking and problem-solving abilities

  • Ability to supervise tactical and technical activities while performing individual tasks

  • Adaptability in a dynamic, global, and regulated environment


Benefits & Compensation

  • Competitive salary with a flexible benefits package

  • Eligibility for Medtronic Incentive Plan (MIP)

  • Opportunities for career growth and professional development

  • Inclusive work environment with a strong focus on employee well-being


Why Join Medtronic

  • Contribute to innovative solutions that positively impact patients worldwide

  • Work in a global organization that values collaboration, diversity, and inclusion

  • Gain exposure to clinical research leadership and regulatory strategy across multiple therapy areas

  • Be part of a company committed to engineering extraordinary solutions for healthcare


Apply Now

Advance your career as a Clinical Research Supervisor at Medtronic and lead clinical research initiatives that drive regulatory compliance, operational excellence, and patient-centered innovation.