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Medical Writing Lead

2 months ago

Wokingham, Wokingham, United Kingdom tranScrip Full time
About the Role

tranScrip Ltd, a leading pharmaceutical consultancy, is seeking a highly experienced Senior Medical Writer to join our team. As a key member of our team, you will be responsible for creating high-quality regulatory, clinical, and scientific content documents for our clients.

Key Responsibilities
  • Develop and maintain a deep understanding of regulatory requirements and industry standards.
  • Collaborate with cross-functional teams to develop and implement medical writing strategies.
  • Prepare and review regulatory documents, including protocols, clinical study reports, and briefing books.
  • Manage and prioritize multiple projects simultaneously, ensuring timely delivery and high-quality output.
  • Provide guidance and support to junior team members, promoting knowledge sharing and skill development.
  • Stay up-to-date with industry trends, regulatory changes, and best practices in medical writing.
Requirements
  • Minimum 5 years of experience as a Regulatory Medical Writer in the pharmaceutical/biotech industry.
  • Proven track record of preparing high-quality regulatory documents without supervision.
  • Excellent project management and planning skills, with the ability to manage budgets and prioritize tasks.
  • Strong analytical and strategic skills, with the ability to interpret complex data and develop effective solutions.
  • Excellent written and oral communication skills, with the ability to communicate complex information to both technical and non-technical audiences.
  • Proficient use of Endnote and internet searches, including PubMed.
What We Offer
  • A competitive base salary and bonus scheme.
  • A comprehensive pension scheme and life assurance.
  • Private health insurance and travel insurance.
  • Retail discounts and a strong focus on continuing professional development (CPD).
Location

This is an office-based role, with some home-working possible for the right candidate.