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Senior Specialist/Expert Medical Writer

4-9 years
Not Disclosed
10 Jan. 6, 2025
Job Description
Job Type: Full Time Education: BPharm/MPharm/PHD/BDS/BSC/MSC/MD/PhD 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

Title: Senior Specialist / Expert Medical Writer
Location: Bangalore


Work Your Magic With Us!

Are you ready to break barriers, explore new horizons, and innovate to enrich lives? Join us in using science and technology to make a difference in Healthcare, Life Science, and Electronics. Together, we imagine the unimaginable, care for people and the planet, and create a world full of possibilities.


About the Role

As a Senior Specialist/Expert Medical Writer, you will play a pivotal role in supporting Medical Writing initiatives for Marketed Products and Lifecycle Management at global and regional/local levels.

Key Responsibilities

  • Independently prepare clinical and regulatory documents such as Protocols, Clinical Study Reports, and Investigator Brochures.
  • Support submissions for market approval or line extensions with minimal supervision.
  • Contribute proactively to the development and implementation of medical writing best practices and process improvements.
  • Oversee and coordinate external writers on documents under your responsibility, ensuring high-quality outputs aligned with business objectives and company standards.
  • Ensure documents meet agreed timelines, adhere to SOPs, and comply with regulatory and company requirements.
  • Maintain consistency, clarity, and proper organization in all documents, with appropriate use of the English language and grammar.
  • Participate in meetings related to medical writing, quality control, and compliance activities.

Who You Are

  • Education: Graduate or postgraduate degree in BPharm/MPharm, PhD, BDS (Dental), BSc/MSc, or equivalent experience.
  • Experience: 4 to 9 years of regulatory medical writing experience, with comprehensive knowledge of theories, principles, and concepts in medical writing.
  • Skills:
    • Excellent written and spoken English, including familiarity with medical terminology and the AMA style guide.
    • Strong knowledge of clinical and regulatory document development.

What We Offer

We are committed to fostering a culture of inclusion and belonging. At our company, we value diversity in all its forms—backgrounds, perspectives, and life experiences. By celebrating diversity, we strengthen our ability to lead in science and technology, delivering excellence and innovation.

Here’s what you can expect:

  • Opportunities to develop and grow at your own pace.
  • A supportive, inclusive environment where you can bring your authentic self to work.
  • A global team of curious minds dedicated to championing human progress.

Equal Opportunity Employer

We believe in equality and inclusion as core values. We are committed to non-discrimination on the basis of race, caste, creed, religion, gender, age, disability, marital status, sexual orientation, or gender identity.


Apply now and join our diverse team to work your magic and make a difference in the world!