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Clinical Evaluation Medical Writer Specialist

4-7 years
Not Disclosed
10 April 29, 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 Specialist
Location: Hybrid, Nanakramguda, Hyderabad, India
Time Type: Full Time
Posted On: 30+ Days Ago
Job Requisition ID: R21455


Job Description

At Medtronic, you have the opportunity to embark on a fulfilling career, driving healthcare innovation while promoting access and equity. We strive for a connected, compassionate world, and we’re looking for passionate individuals to help us reach that goal.

A Day in the Life

As a Clinical Evaluation Medical Writer Specialist-II, your responsibilities will include:

  • Reviewing and summarizing scientific literature.

  • Reporting instances of complaints or adverse events from literature to GCH.

  • Creating responses for audit/submission queries.

  • Maintaining a database of peer-reviewed literature.

  • Appraising, analyzing, summarizing, and discussing clinical evidence.

  • Conducting comprehensive literature searches and critical evaluations of clinical evidence.

  • Developing up-to-date reports on product families for their intended purpose.

  • Creating and maintaining plans and reports for regulatory authorities.

  • Reviewing and approving documentation for device development.

  • Ensuring adherence to regulatory agency guidelines for clinical evaluations.

Qualifications

Minimum Qualifications

  • Bachelor’s degree in Medical, Mechanical, Electrical Life Sciences, or a Master’s in Pharmaceutical Sciences.

  • 4-7 years of experience as a medical/clinical writer in the medical device and/or pharmaceutical industry (a mix of both is preferred).

  • Excellent written, organizational, and communication skills.

  • Ability to manage multiple tasks efficiently while adhering to deadlines.

  • Proficiency in English (reading, writing, speaking).

  • Strong attention to detail and good planning abilities.

  • A flexible, team-oriented attitude and a good learning attitude.

Key Differentiating Factors

  • Autonomy: Works independently with general supervision on larger, moderately complex projects.

  • Organizational Impact: Contributes to project milestones and may be involved in cross-functional assignments.

  • Innovation and Complexity: Handles general issues with an understanding of broader issues, suggesting enhancements to systems and processes.

  • Communication and Influence: Communicates with internal contacts to share information and support decision-making.

  • Leadership and Talent Management: May mentor entry-level professionals or assist others in the career stream.

About Medtronic

Medtronic is committed to transforming healthcare worldwide. We tackle the most challenging health problems with innovative solutions. Our mission—to alleviate pain, restore health, and extend life—guides our team of 95,000+ passionate individuals. Join us in shaping the future of healthcare.

Benefits & Compensation

Medtronic offers competitive salaries and flexible benefits packages. We value the contributions of our employees and provide resources and compensation designed to support their career and life stages.