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Associate Clinical Data Specialist - Mumbai

Medtronic
Medtronic
3+ years
Not Disclosed
Mumbai, India
10 March 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Position Summary
The Associate Clinical Data Specialist is responsible for supporting clinical data management activities related to clinical trials and data collection studies. The role focuses on designing, implementing, and maintaining clinical data systems while ensuring high-quality data collection and validation across clinical studies.

This position collaborates with cross-functional teams to support clinical protocol design, database development, and data review processes to ensure accurate and reliable clinical trial data.

Key Responsibilities

Collaborate with internal teams to design, document, test, and implement clinical data collection systems for clinical studies

Support the design and implementation of clinical protocols and data collection frameworks

Develop and maintain systems for organizing and analyzing clinical data and identifying trends

Manage clinical data management issues by reviewing study protocols and ensuring consistency across projects

Design and standardize Case Report Form (CRF) modules to support clinical study objectives

Develop and implement data quality management plans for clinical trials

Provide early strategic input into protocol development with a focus on data management considerations

Review and resolve clinical data discrepancies using standardized validation procedures

Prepare clinical study reports and documentation for internal validation and cross-validation studies

Collaborate with stakeholders to ensure effective data collection, analysis, and reporting throughout clinical trial execution

Professional Experience Requirements

Minimum 3 years of experience in clinical data management or related clinical research roles

Experience designing and managing clinical databases and data collection systems

Knowledge of clinical trial processes and clinical data validation procedures

Experience reviewing clinical protocols and managing CRF modules

Strong analytical and organizational skills for managing clinical datasets

Ability to collaborate effectively with cross-functional teams involved in clinical research

Apply Details

Apply via the company career portal for
Medtronic