Senior Medical Writer

5 days ago


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

We are seeking a highly experienced Senior Medical Writer to join our team at tranScrip Ltd, a leading pharmaceutical consultancy. As a Senior Medical Writer, you will play a key role in supporting our clients globally, providing strategic expertise and therapeutic experience across the entire product lifecycle.

Key Responsibilities
  • Develop high-quality regulatory, clinical, and scientific content documents, including regulatory dossier elements, protocols, clinical study reports, and briefing books.
  • Manage multiple projects simultaneously, prioritizing tasks and meeting deadlines.
  • Collaborate with cross-functional teams, including therapeutic and development teams, to ensure seamless project execution.
  • Identify, interview, and recommend subcontractor Medical Writers, as well as manage their project work.
  • Support the development of client proposals, ensuring scope, quality, time, and cost are met.
  • Lead or support key business initiatives, training, and mentoring junior team members.
Requirements
  • Minimum 5 years' experience as a Regulatory Medical Writer in the pharmaceutical/biotech industry, ideally in a CRO environment.
  • Proven track record in preparing clinical and regulatory documents without supervision.
  • Excellent project management and planning skills, with the ability to manage budgets.
  • Experience in a wide range of indications and proficiency in Endnote and internet searches, including PubMed.
  • Life science degree, preferably a higher degree (e.g., MSc, PhD).
What We Offer
  • Competitive base salary and bonus scheme.
  • Pension scheme, life assurance, and group income protection.
  • Private health insurance and travel insurance.
  • Retail discounts and a strong focus on CPD.
Location

The position is office-based, with some home-working possible for the right candidate. Remote work is also an option.



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