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Assoc Clinical Data Spec

Medtronic
Medtronic
0-2 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

Job Title: Associate Clinical Data Specialist
Location: Chennai Kilpauk, Tamil Nadu, India (Remote)
Job Type: Full-Time
Job ID: R55390
Posted: 21 Days Ago

Company Overview:
Medtronic is a global leader in healthcare technology, dedicated to alleviating pain, restoring health, and extending life. With a team of 95,000+ professionals worldwide, we drive innovation to tackle complex health challenges, delivering real solutions for real people. At Medtronic, employees are empowered to experiment, create, and implement ideas that improve lives across the globe.

Position Overview:
We are seeking a detail-oriented Associate Clinical Data Specialist to support clinical data management initiatives. This role involves collaborating with cross-functional teams to design, implement, and maintain clinical data collection systems, ensuring the accuracy, consistency, and integrity of data across clinical studies. This position is ideal for early-career professionals seeking to grow in the clinical data management field.

Key Responsibilities:

  • Collaborate with internal departments to design, document, and implement clinical data collection protocols and databases.

  • Develop and maintain systems for organizing, analyzing, and reporting clinical data trends.

  • Identify and resolve data discrepancies, ensuring compliance with standard validation procedures.

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

  • Manage cross-project consistency in case report forms (CRFs) and develop data quality plans.

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

  • Support project delivery from design through implementation, adhering to established policies and procedures.

Required Qualifications & Experience:

  • Bachelor’s degree in Life Sciences, Pharmacy, or a related field (or equivalent international qualification).

  • 0–2 years of experience in clinical data management, clinical research, or related roles preferred.

  • Strong analytical, organizational, and problem-solving skills.

  • Familiarity with clinical trial processes, CRFs, and data validation practices is advantageous.

  • Effective communication skills and the ability to work collaboratively in cross-functional teams.

Career Level & Impact:

  • Entry-level individual contributor role with close supervision.

  • Responsible for smaller, less complex projects within the clinical data management function.

  • Opportunity to gain exposure to clinical protocols, data collection systems, and cross-functional collaboration.

Benefits & Compensation:

  • Competitive salary and comprehensive benefits package.

  • Eligible for the Medtronic Incentive Plan (MIP).

  • Opportunities for professional development, mentorship, and career growth.

  • Flexible work environment with a focus on work-life balance.

Why Medtronic:
Join a company that champions healthcare access and equity worldwide. Medtronic empowers employees to innovate, create, and make a tangible impact on patient outcomes. Be part of a global team that values diversity, inclusion, and personal growth.

Apply Today:
If you are passionate about clinical data management and eager to build a career in a leading healthcare technology company, apply now to join Medtronic as an Associate Clinical Data Specialist.