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Regulatory Medical Writing Lead
2 months ago
tranScrip Ltd, a leading pharmaceutical consultancy, is seeking a highly experienced Senior Medical Writer to join our team. As a Senior Medical Writer, you will play a crucial role in creating high-quality regulatory, clinical, and scientific content documents for our clients.
Key Responsibilities- Project Writing: Develop and manage projects from start to finish, ensuring timely delivery of high-quality documents.
- Client Management: Collaborate with clients and internal teams to understand project requirements and deliverables.
- Team Leadership: Mentor and guide junior team members, providing guidance and support to ensure successful project outcomes.
- Business Development: Contribute to business development efforts by identifying new opportunities and building relationships with clients and partners.
- Experience: Minimum 5 years of experience as a Regulatory Medical Writer in the pharmaceutical/biotech industry, with a proven track record of delivering high-quality documents.
- Education: Life science degree, preferably a higher degree (e.g. MSc, PhD).
- Skills: Excellent project management and planning skills, with the ability to manage budgets and prioritize tasks. Proficient use of Endnote and internet searches, including PubMed.
- Competitive Salary: A competitive base salary and bonus scheme.
- Benefits: A comprehensive benefits package, including pension scheme, life assurance, group income protection, private health insurance, and travel insurance.
- Professional Development: Opportunities for professional development and growth within the company.