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Clinical Evaluation Medical Writer

0-2 years
₹9 – 14 LPA
10 Aug. 21, 2025
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

Job Title: Clinical Evaluation Medical Writer
Location: Remote (India – Mumbai preferred)
Company: Medtronic
Job Type: Full-Time
Job ID: R37182

About the Company:
Medtronic is a global leader in healthcare technology, committed to alleviating pain, restoring health, and extending life. With 95,000+ employees worldwide, Medtronic engineers life-transforming solutions that redefine how healthcare challenges are addressed.

Role Overview:
As a Clinical Evaluation Medical Writer, you will play a critical role in compiling, analyzing, and presenting clinical evidence for medical devices, ensuring compliance with global regulatory standards. This role requires strong literature evaluation, scientific writing, and regulatory knowledge to support submissions and product development.

Key Responsibilities:

  • Review, appraise, and summarize scientific literature.

  • Conduct comprehensive literature searches and evaluate clinical evidence.

  • Prepare Clinical Evaluation Reports (CERs), plans, and related regulatory documentation.

  • Report literature-based complaints and adverse events to the Global Complaint Handling (GCH) system.

  • Develop state-of-the-art documents for product families aligned to intended purposes.

  • Maintain and update databases of peer-reviewed literature.

  • Draft responses for audits and regulatory authority queries.

  • Review and approve supporting documentation for device development.

  • Collaborate with cross-functional stakeholders on medical writing deliverables.

  • Stay current with global regulatory guidelines (e.g., EU MDR, MEDDEV, FDA) for clinical evaluation.

Qualifications:

  • Bachelor’s degree in Life Sciences, Medicine, Pharmacy, or related field (required).

  • Minimum 2 years’ relevant experience in medical writing or clinical evaluation.

  • Advanced degree (Master’s/PhD) preferred; may substitute for experience.

  • Strong knowledge of regulatory requirements for clinical evaluation (e.g., EU MDR, MEDDEV 2.7/1 Rev 4).

  • Proven ability to appraise and critically analyze clinical evidence.

  • Excellent written and verbal communication skills.

  • Ability to work independently with minimal supervision.

Core Competencies:

  • Strong scientific and analytical mindset.

  • Detail-oriented with structured documentation skills.

  • Ability to balance multiple priorities in a regulated environment.

  • Collaborative mindset with mentoring potential.

Compensation & Benefits:

  • Competitive salary (₹9 – 14 LPA, based on Indian market benchmarks for mid-level medical writers).

  • Flexible benefits package supporting career growth and work-life balance.

  • Professional development and continuous learning opportunities.

Why Join Medtronic?

  • Contribute to life-transforming technologies impacting millions of patients worldwide.

  • Work with a diverse, global team of innovators.

  • Access to inclusive culture, leadership support, and long-term career growth.

  • Be part of a mission-driven company engineering extraordinary solutions in healthcare.