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Clinical Studies Spt Coord Ii

Medtronic
Medtronic
2+ years
Not Disclosed
10 Jan. 9, 2026
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 Studies Support Coordinator II

Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Job ID: R47906


About the Role

Medtronic is seeking a Clinical Studies Support Coordinator II to provide operational and administrative support for clinical studies. This role focuses on data coordination, document management, and process compliance, with moderate autonomy and scope to contribute to clinical study efficiency.

This position is ideal for professionals with 2+ years of experience in clinical operations, clinical data management, or study coordination who are looking to advance in a global medical technology organization.


Key Responsibilities

  • Clinical Data Coordination:

    • Participate in the development and testing of case report forms (CRFs), study databases, and study reports according to protocol requirements.

    • Ensure timely and accurate completion of data forms and resolve data discrepancies.

    • Support compensation processing and manage discrepancies as needed.

  • Document Management:

    • Create, organize, and maintain clinical study files.

    • Oversee distribution of study documents and assist in periodic audits for completeness and compliance.

  • Process Support & Problem Solving:

    • Perform routine administrative and clerical tasks while suggesting minor adjustments to improve work processes.

    • Highlight operational issues and propose solutions within the scope of the role.

  • Team Support:

    • Provide guidance and assistance to new or entry-level team members as required.

    • Communicate effectively with internal contacts and cross-functional teams to ensure smooth study execution.


Required Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, or related field.

  • Minimum 2 years of relevant experience in clinical study coordination or clinical data management.

  • Proficiency in Microsoft Office and basic clinical systems.

  • Strong organizational, problem-solving, and communication skills.

  • Ability to work under moderate supervision with attention to detail and adherence to study protocols.


What Medtronic Offers

  • Competitive salary and flexible benefits package.

  • Eligibility for Medtronic Incentive Plan (MIP).

  • Opportunity to work on global clinical trials with exposure to advanced clinical processes.

  • Career growth opportunities in a leading healthcare technology organization.


About Medtronic

Medtronic is a global leader in medical technology, dedicated to alleviating pain, restoring health, and extending life. With over 95,000 employees worldwide, Medtronic combines innovation, expertise, and compassion to solve the world’s most challenging healthcare problems.

Join Medtronic to advance your career while impacting patient outcomes worldwide, contributing to high-quality clinical research and operational excellence.