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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 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 (Remote)
Job Type: Full-Time
Job ID: R55535


About the Role

Medtronic is seeking a Clinical Studies Support Coordinator II to support the execution and management of clinical studies. This role involves coordinating clinical data, documentation, and administrative processes to ensure studies are conducted efficiently, accurately, and in compliance with regulatory and protocol requirements. The position is remote, providing flexibility while engaging with global teams.

This role is ideal for professionals with 2+ years of relevant experience in clinical operations, clinical data management, or study coordination seeking to advance their career in a leading global healthcare technology organization.


Key Responsibilities

  • Clinical Data Coordination:

    • Participate in the development and testing of case report forms (CRFs), study reports, and databases based on protocol specifications.

    • Verify study data, manage discrepancies, and ensure timely and accurate completion of data forms.

    • Support compensation processes, including identifying and resolving discrepancies.

  • Clinical Document Management:

    • Create, organize, and maintain clinical study files.

    • Distribute study documents and ensure completeness and accuracy during periodic audits.

  • Process and Administrative Support:

    • Apply prior experience to clerical and administrative tasks while working under moderate supervision.

    • Highlight areas of concern in current processes and propose solutions.

    • Assist new or entry-level team members in understanding workflows and procedures.

  • Communication & Collaboration:

    • Liaise with internal teams across Medtronic to provide information, guidance, and updates.

    • Ensure that information shared is accurate and follows organizational protocols.


Required Qualifications & Experience

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

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

  • Strong organizational skills and attention to detail.

  • Ability to work independently and collaboratively within cross-functional teams.

  • Proficiency in Microsoft Office and clinical data systems.

  • Excellent written and verbal communication skills in English.


What Medtronic Offers

  • Competitive salary and benefits package.

  • Eligibility for the Medtronic Incentive Plan (MIP).

  • Opportunity to work remotely while contributing to global clinical operations.

  • Career growth in a leading medical technology company committed to innovation, inclusion, and patient impact.

  • Exposure to global clinical trial processes and regulatory compliance standards.


About Medtronic

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

At Medtronic, you will grow your career while making a tangible impact on patients’ lives, collaborating with diverse teams, and engaging in cutting-edge clinical studies.


Apply now to be part of a dynamic team driving innovation in clinical research and healthcare solutions.