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Clinical Research Supervisor

Medtronic
Medtronic
1-3 years
Not Disclosed
10 Dec. 31, 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 – Remote

Location: Mumbai, Maharashtra, India
Work Mode: Remote
Employment Type: Full-Time
Job Requisition ID: R54470
Posted: 21 Days Ago
Company: Medtronic


About Medtronic

Medtronic is a global leader in healthcare technology, driven by a mission to alleviate pain, restore health, and extend life. With a workforce of over 95,000 professionals worldwide, Medtronic develops innovative medical solutions that address some of the most complex health challenges facing humanity. The organization fosters a culture of purpose-driven leadership, innovation, diversity, and inclusion.


Job Overview

The Clinical Research Supervisor will provide leadership and operational oversight for the conduct of clinical studies and related regulatory activities supporting product approvals. This role ensures that all clinical research activities are scientifically sound, ethically conducted, and compliant with global regulatory requirements. The position involves managing local and global clinical research projects, supervising team members, and acting as a key clinical research representative within the region.


Key Responsibilities

  • Provide leadership for the planning, execution, and oversight of clinical studies across multiple therapeutic areas.

  • Ensure clinical studies are scientifically valid, ethically conducted, and compliant with applicable regulatory standards and guidelines.

  • Deliver accurate and timely assessments of product safety and efficacy to support regulatory submissions and product approvals.

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

  • Ensure accuracy, completeness, and compliance of clinical and regulatory submissions.

  • Lead execution of both local and global clinical research projects across multiple Medtronic business units.

  • 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 communicate feedback from local customers and regulatory bodies to internal teams.


People Management and Leadership

  • Supervise and manage a team of clinical research professionals, typically with six or more direct reports.

  • Provide day-to-day operational direction, workload planning, and resource allocation to ensure productivity and compliance.

  • Mentor, coach, and develop team members to meet or exceed performance expectations.

  • Conduct regular one-on-one meetings, performance reviews, and development planning discussions.

  • Support hiring, promotion, performance evaluation, and reward decisions for direct reports.

  • Drive engagement, inclusion, and alignment with departmental and organizational objectives.


Differentiating Factors

Autonomy:

  • Provides tactical and technical supervision while also contributing individually to assigned tasks.

  • Operates within established procedures while delivering results independently.

Organizational Impact:

  • Plans and manages operational objectives for a defined team or department.

  • Influences team schedules, resource allocation, and operational priorities.

  • May manage day-to-day budget elements such as staffing or overtime, without full P&L responsibility.

Innovation and Complexity:

  • Identifies process improvements and recommends enhancements to systems and workflows.

  • Addresses defined problems requiring understanding of broader operational and regulatory considerations.

Communication and Influence:

  • Communicates effectively with internal teams, external partners, vendors, and regulatory stakeholders.

  • Presents and exchanges information to support informed decision-making and problem resolution.


Required Qualifications and Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related scientific discipline.

  • Minimum of 1–3 years of relevant experience in clinical research, clinical operations, regulatory affairs, or related healthcare roles.

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

  • Foundational people management skills, including work scheduling, prioritization, coaching, and performance management.

  • Broad technical and operational knowledge within the clinical research domain.

  • Strong organizational, communication, and leadership skills.


Physical Job Requirements

This role involves standard office and remote working conditions. The responsibilities described represent the general nature of the position and are not an exhaustive list of all duties and skills required.


Benefits and Compensation

Medtronic offers a competitive salary and a comprehensive, flexible benefits package designed to support employees at every stage of their career and life. Employees are eligible for a short-term incentive under the Medtronic Incentive Plan (MIP), in addition to other benefits and resources that recognize individual and team contributions.


Why Join Medtronic

At Medtronic, innovation is powered by purpose. Employees collaborate across disciplines to create meaningful healthcare solutions that improve lives globally. From research and development to clinical execution and regulatory strategy, Medtronic provides opportunities to grow, lead, and make a lasting impact.