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Clinical Studies Spt Coord Ii

Medtronic
Medtronic
2+ years
Not Disclosed
10 Jan. 19, 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 Studies Support Coordinator II
Location: Mumbai, Maharashtra, India
Employment Type: Full-Time
Job ID: R47906
Posted: 27 Days Ago

About the Role
Medtronic is seeking a Clinical Studies Support Coordinator II to provide essential support for clinical studies. This role ensures accurate data management, document organization, and operational efficiency while maintaining compliance with regulatory standards. It is ideal for professionals with experience in clinical research, healthcare data coordination, and clinical documentation.

Key Responsibilities

  • Support clinical studies in one or more operational areas:

    • Data Coordination: Develop and test case report forms, study databases, and study reports based on protocol requirements. Verify data, resolve discrepancies, and ensure timely completion of data forms.

    • Document Coordination: Create, manage, and organize clinical study files. Oversee the distribution and completeness of clinical study documents. Conduct periodic audits to ensure accuracy.

    • Compensation Processing: Identify and resolve compensation discrepancies when applicable.

  • Execute routine administrative and clerical tasks with moderate supervision, making minor adjustments to improve processes.

  • Communicate effectively with internal stakeholders to provide explanations or interpretations of study data and procedures.

  • Highlight areas of concern within the workstream and propose practical solutions.

  • Provide guidance and support to new or entry-level employees as needed.

Experience and Skills Required

  • Minimum 2 years of relevant experience in clinical study support, data coordination, or document management in the healthcare, clinical research, or medical device sector.

  • Solid knowledge of clinical study procedures, regulatory standards, and documentation requirements.

  • Ability to manage multiple tasks efficiently and work under moderate supervision.

  • Proficiency in data verification, discrepancy resolution, and clinical file audits.

  • Strong communication skills and ability to collaborate effectively across teams.

Education

  • Bachelor’s degree in Life Sciences, Clinical Research, Healthcare Administration, or a related field is required.

Benefits & Compensation
Medtronic offers a competitive salary and flexible benefits package designed to support employees at every stage of their career. This role is eligible for the Medtronic Incentive Plan (MIP).

About Medtronic
Medtronic is a global leader in healthcare technology, addressing the world’s most critical health challenges. Our mission—to alleviate pain, restore health, and extend life—drives a diverse team of 95,000+ professionals committed to delivering innovative solutions across R&D, manufacturing, and clinical practice. We foster a culture of inclusion, collaboration, and continuous improvement to create meaningful impact worldwide.

How to Apply
Join Medtronic and contribute to advancing clinical research with precision, compliance, and operational excellence. Apply today to be part of a global team dedicated to healthcare innovation.