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Medical Writer Group Lead

8-12 years
Not Disclosed
10 April 28, 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

Medical Writer Group Lead

Department:
Drug Safety Services

Employment Type:
Full-Time

Minimum Experience:
Experienced

Location:
Mysore, Karnataka

Description:
As a Medical Writer Group Lead, you will play a pivotal role in the development of high-quality clinical and regulatory documents across multiple therapeutic areas. Collaborating closely with sponsors and internal cross-functional teams, you will be responsible for authoring and delivering key documents such as Clinical Study Reports (CSRs), Patient Narratives, Investigator’s Brochures (IBs), Protocols, and additional documentation to support end-to-end clinical trial processes and regulatory submissions.

Key Responsibilities:

  • Prepare, write, and review a range of clinical and regulatory documents in compliance with ICH-GCP guidelines, sponsor-specific templates, and global regulatory standards.

  • Deliver accurate, high-quality, and scientifically sound documents, including:

    • Clinical Study Reports (CSRs)

    • Patient Safety Narratives

    • Investigator’s Brochures (IBs)

    • Clinical Study Protocols and Amendments

    • Protocol Synopses, Clinical Trial Summaries, and other regulatory submission documents

  • Interpret and present clinical data from statistical tables, listings, and figures.

  • Liaise with cross-functional teams such as clinical, biostatistics, pharmacovigilance, and project management to ensure timely and accurate document delivery.

  • Communicate effectively with sponsor teams, incorporating feedback and managing revisions.

  • Maintain version control and ensure adherence to project timelines, SOPs, and internal quality standards.

Qualifications:

  • Bachelor’s, Master’s, or PhD in Life Sciences, Pharmacy, Medicine, or a related field.

  • Minimum 8–12 years of medical writing experience within a CRO or a clinical research environment.

  • Demonstrated knowledge of ICH guidelines and global regulatory requirements.

  • Proficient in MS Office Suite (Word, Excel, PowerPoint) and familiar with document management systems.

  • Strong written and verbal communication skills.

  • Excellent analytical and organizational abilities with proven capability to manage multiple projects simultaneously.

Preferred:

  • Experience with eCTD submissions and regulatory agency interactions.

  • Familiarity with therapeutic areas such as oncology, CNS, cardiovascular, or rare diseases.

  • Knowledge of tools like Adobe Acrobat Pro and referencing software.