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Senior Medical Regulatory Writer

5+ years
Not Disclosed
10 Dec. 13, 2024
Job Description
Job Type: Full Time Education: PhD/BSc/MSc/DPharma/PharmD/MBBS/BDS/BAMS/BHMS/MD 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: Medical Writer (Regulatory)
Location: Hyderabad / Mumbai
Job Type: Permanent, Full-time
Hiring Manager: Head, Scientific Communications / Team Lead
Travel: Travel required as per business need

About Sanofi Global Hub

Sanofi Global Hub, based in India, is a centralized resource organization that supports a wide range of functions including Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, and Data & Digital. The Global Hub aims to be a strategic and functional partner for tactical deliveries to Sanofi's Medical, HEVA, and Commercial organizations worldwide.

Main Responsibilities

As a Medical Writer at Sanofi, you will play a key role in producing high-quality medical and regulatory documents. You will be responsible for drafting and editing the medical sections of critical documents such as:

  • Periodic Benefit-Risk Evaluation Reports (PBRERs)
  • Clinical Study Reports (CSR)
  • Addendum to Clinical Overviews
  • Product and Disease ID Cards
  • Clinical Evaluation Reports
  • Product Alerts
  • Trial Transparency Documents

You will ensure these documents meet internal and external standards and guidelines, are delivered on time, and are aligned with regulatory requirements.

Key Duties and Responsibilities:

  1. Medical Writing & Document Creation:

    • Author and edit high-quality clinical and safety documents.
    • Contribute to Periodic Benefit-Risk Evaluation Reports (PBRER), Clinical Study Reports (CSR), Addendums to clinical overviews, and other regulatory documents.
    • Collaborate effectively with cross-functional teams to produce accurate and comprehensive documents.
  2. Collaboration with Stakeholders:

    • Work with Medical, Regulatory, Pharmacovigilance, and Clinical teams to ensure documents are aligned with business needs and regulatory requirements.
    • Proactively liaise with the relevant teams (Scientific communication, Medical regulatory writing, etc.) to prepare customized documents.
  3. Document Review & Mentoring:

    • Review and provide feedback on documents created by peer writers.
    • Mentor and support junior medical writers, assisting with their professional development.
  4. Regulatory Compliance:

    • Maintain awareness of regulatory requirements across multiple regions (FDA, EU, etc.).
    • Ensure all documents comply with ICH, GCP, GVP, and internal standards.
    • Prepare and review documents for audit and inspection readiness.
  5. Stakeholder Engagement:

    • Maintain relationships with key stakeholders within the allocated business unit.
    • Collaborate with external vendors to meet deliverable timelines and quality standards.
  6. Product and Trial Information Management:

    • Oversee the preparation and posting of trial-related information on public databases (e.g., CTG, EUCTR, EUDRACT).
    • Track postings, archive materials in relevant systems, and ensure data is up-to-date.
  7. Continual Improvement:

    • Participate in developing new strategies to improve document delivery and content quality.
    • Contribute to the development of regulatory writing strategies for assigned products and therapeutic areas.

About You

Experience:

  • >5 years of experience in regulatory writing in the pharmaceutical or healthcare industry. Experience in writing medical and clinical documents such as PBRER, CSR, and other regulatory submissions is preferred.

Education:

  • Advanced degree in life sciences, pharmacy, or a similar discipline (e.g., PhD, Master’s, or Bachelor’s in Science, D Pharma, PharmD).
  • Medical degree (e.g., MBBS, MD, BDS, BHMS) would be a plus.

Skills:

  • Stakeholder management and ability to work collaboratively with cross-functional teams.
  • Excellent writing and editing skills with the ability to summarize scientific information clearly for specific audiences.
  • Strong knowledge of ICH, GCP, GVP, and regulatory compliance.
  • Data interpretation and medical literature screening.
  • Ability to work independently and within a team environment.
  • Proficiency in computer applications relevant to medical writing.

Languages:

  • Fluent in English, with excellent written and verbal communication skills.

Why Sanofi?

At Sanofi, we believe in pursuing progress through collaboration and innovation. We are committed to providing equal opportunities and fostering an inclusive, diverse workplace. Join us to make a meaningful impact in the world of healthcare.

Pursue Progress. Discover Extraordinary.

Sanofi is an equal opportunity employer, providing opportunities for all individuals, regardless of race, gender, nationality, or background. Explore more about our Diversity, Equity, and Inclusion initiatives at Sanofi.