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Associate Clinical Data Specialist - Mumbai

3+ years
Not Disclosed
10 Nov. 13, 2025
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

Associate Clinical Data Specialist

📍 Location: Mumbai, Maharashtra, India
🕒 Type: Full-time
📅 Posted: 7 Days Ago
📄 Requisition ID: R50296
🏢 Company: Medtronic


About Medtronic

At Medtronic, you can begin a life-long career of exploration and innovation, helping champion healthcare access and equity for all. You’ll lead with purpose — breaking barriers to innovation in a more connected, compassionate world.


Position Summary

The Associate Clinical Data Specialist is responsible for supporting the design, documentation, testing, and implementation of clinical data collection systems and databases. The role collaborates cross-functionally to ensure data integrity, compliance, and efficiency in clinical studies.


Key Responsibilities

  • Collaborate with various departments in the design, documentation, testing, and implementation of clinical data collection studies.

  • Design and implement clinical protocols and data collection systems.

  • Develop systems to organize, analyze, identify, and report data and trends.

  • Manage data management issues by ensuring cross-project consistency and identifying standard Case Report Form (CRF) modules.

  • Develop and maintain data quality plans.

  • Provide strategic input into protocol design with a focus on data management.

  • Review and resolve data discrepancies using standardized validation systems and procedures.

  • Prepare clinical trial reports for internal validation and cross-validation studies.


Career Stream – Specialist

  • Role Type: Individual contributor (professional discipline or specialty).

  • Work Focus: Delivering and managing assigned projects, from design to implementation.

  • Mentorship: May mentor colleagues or guide lower-level professionals.

  • Supervision: Works under close supervision; autonomy increases with experience.


Differentiating Factors

Category

Description

Autonomy

Entry-level contributor; works with close supervision.

Organizational Impact

Delivers work of limited scope; small or less complex projects.

Innovation & Complexity

Solves straightforward problems; may make minor process improvements.

Communication & Influence

Communicates mainly with internal team members; gathers and conveys information.

Leadership

No formal leadership; focuses on self-development.

Knowledge Required

Broad theoretical job knowledge gained through advanced education.


Qualifications

  • Minimum 3+ years of experience in Clinical Data Management.

  • Strong understanding of clinical databases, CRF design, and data validation systems.

  • Excellent analytical, documentation, and communication skills.

  • Ability to work in a collaborative team environment and manage priorities effectively.


Physical Job Requirements

The responsibilities and physical demands described here represent the general nature and level of work expected of employees in this role. They are not exhaustive of all duties and skills required.


Compensation & Benefits

  • Competitive salary and flexible benefits package.

  • Medtronic Incentive Plan (MIP): Short-term performance-based incentive eligibility.

  • Comprehensive career and life-stage support, including wellness, insurance, and professional development programs.

  • Recognition and rewards for contributions to company success.