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Associate Clinical Data Specialist - Mumbai

Medtronic
Medtronic
3+ years
Not Disclosed
10 Jan. 19, 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
Location: Mumbai, Maharashtra, India (Remote Work Option Available)
Employment Type: Full-Time
Job ID: R50296
Posted: 28 Days Ago

About the Role
Medtronic is seeking an Associate Clinical Data Specialist to support clinical data management activities across multiple clinical studies. This role is ideal for professionals with experience in clinical data collection, protocol implementation, and data quality assurance within the healthcare or medical device industry.

Key Responsibilities

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

  • Design and implement clinical protocols and data collection systems to ensure accurate and timely capture of study data.

  • Develop systems for organizing, analyzing, and reporting data trends to support decision-making and study outcomes.

  • Manage data management issues by reviewing protocols for cross-project consistency and identifying standard Case Report Form (CRF) modules to meet objectives.

  • Develop and maintain data quality plans to ensure compliance with internal and regulatory standards.

  • Provide strategic input early in protocol design, focusing on data management considerations.

  • Review and resolve data discrepancies in line with standardized validation systems and procedures.

  • Prepare reports for internal validation, cross-validation, and study documentation purposes.

  • Act as a mentor or resource for colleagues when required, contributing to team knowledge sharing.

Experience and Skills Required

  • Minimum 3 years of experience in clinical data management or related clinical research functions.

  • Strong understanding of clinical protocols, data collection, and database management in healthcare or medical device research.

  • Ability to design, implement, and manage clinical data systems and processes.

  • Experience in reviewing data discrepancies and ensuring data quality in compliance with regulatory and internal standards.

  • Proficiency in reporting, data analysis, and trend identification.

  • Strong collaboration and communication skills, with the ability to work effectively across teams.

Education

  • Bachelor’s degree in Life Sciences, Clinical Research, Data Science, or related field is required.

Benefits & Compensation
Medtronic provides a competitive salary with a flexible benefits package designed to support professional and personal growth. This role is eligible for the Medtronic Incentive Plan (MIP).

About Medtronic
Medtronic is a global leader in healthcare technology, tackling the most challenging health problems worldwide. Our mission—to alleviate pain, restore health, and extend life—guides a team of 95,000+ professionals who innovate across R&D, manufacturing, and clinical practice. We foster a culture of inclusion, collaboration, and continuous improvement to create meaningful global impact.

How to Apply
Join Medtronic and contribute to the advancement of clinical research with precision, compliance, and operational excellence. Apply today to become part of a global team committed to healthcare innovation.