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Associate Clinical Data Specialist - Mumbai

Medtronic
Medtronic
3+ 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

Associate Clinical Data Specialist – Mumbai, India

Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Job ID: R50296


About the Role

Medtronic is seeking an Associate Clinical Data Specialist to provide professional support for clinical data management in ongoing and upcoming clinical trials. This role is ideal for candidates with 3+ years of experience in clinical data management, data collection, and database validation who are looking to work in a global healthcare technology organization.

The role requires collaboration across clinical operations, data management, and quality teams, ensuring accurate and timely management of clinical trial data while adhering to regulatory and internal standards.


Key Responsibilities

  • Clinical Data Management:

    • Collaborate with cross-functional teams on the design, testing, and implementation of clinical data collection systems.

    • Develop and implement clinical protocols, standardized Case Report Forms (CRFs), and data validation procedures.

    • Review and resolve data discrepancies to ensure consistency and integrity across clinical databases.

    • Contribute early strategic input to protocol design focused on data management considerations.

  • Data Analysis & Reporting:

    • Organize and analyze clinical trial data, identify trends, and prepare reports for internal validation and cross-validation studies.

    • Develop and maintain data quality plans to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

  • Project Support:

    • Assist in managing data management issues and implement minor process improvements for efficiency.

    • Act as a professional resource to colleagues, providing guidance on project-related clinical data management tasks.


Required Qualifications & Experience

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

  • Minimum 3 years of relevant experience in clinical data management within pharmaceutical, biotechnology, or CRO environments.

  • Strong knowledge of clinical trial data systems, data validation, and quality control processes.

  • Proficient in Microsoft Office and clinical database tools.

  • Excellent analytical, organizational, and communication skills.

  • Ability to work independently under supervision and adhere to timelines and quality standards.


What Medtronic Offers

  • Competitive salary and flexible benefits package.

  • Eligibility for Medtronic Incentive Plan (MIP).

  • Exposure to global clinical trials and advanced healthcare technology.

  • Opportunities for professional growth and career advancement within a leading medical technology company.


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 delivers innovative solutions across R&D, manufacturing, and patient care.

Join Medtronic to advance your career while contributing to high-quality clinical research, supporting patient outcomes worldwide, and being part of a culture driven by innovation, collaboration, and impact.