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Senior Medical Content Specialist
2 months ago
About the Role
tranScrip Ltd, a highly specialist pharmaceutical consultancy, is seeking a highly experienced Senior Medical Writer to join their team. This is a dynamic role with a varied workload in a rapidly expanding company.
Key Responsibilities
- Develop high-quality regulatory, clinical, and scientific content documents for a diverse array of clients and projects.
- 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 and recommend subcontractor Medical Writers, managing their project work from a scope, quality, time, and cost basis.
- Support the development of client proposals, ensuring scope, cost, and quality are met.
- Lead or support key business initiatives and training programs.
- Assist project teams and colleagues as needed, providing guidance and mentorship to 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).
- Strong analytical and strategic skills, with excellent written and oral communication skills.
- Good knowledge of local and national guidance and regulations relevant to medical and regulatory writing.
Benefits
- Permanent contract of employment.
- Competitive base salary.
- Bonus scheme.
- Pension scheme.
- Life assurance.
- Group income protection.
- Private health insurance and travel insurance.
- Retail discounts.
- Strong focus on Continuing Professional Development (CPD).