Responsibilities

• Support with the development, review and optimisation of scientifically accurate fair balanced content across a range of formats and audiences (e.g. HCP, patient or payer educational materials, and support for commercial programs and marketing campaigns).
• Research, write, edit and proof scientifically accurate content for a range of channels, including HCP (Health Care Professional) education, sales training presentations and digital communications.
• Translate complex scientific data into clear, compelling and audience-appropriate communications for healthcare professionals and broader audiences where relevant.
• Support early phase narratives for clinical pipeline, translating complex data into clear, compliant medical narratives and support pre-launch disease state materials.
• Support marketing as scientific SME and apply rigour to commercial content, ensuring messaging and claims are credible, evidence based and consistent with labelling.
• Develop and share scientific content, this includes ideation, writing, asset development and delivery through various channels.
• Extract and support commercial and educational messaging from scientific literature and collaborating with product and product trainers in the appropriate usage and delivery of this content.
• Define and evolve the scientific communications approach, ensuring alignment with both medical strategy and business priorities, while maintaining the appropriate separation between medical vs promotional activities and content.
• Act as the subject matter expert for scientific content, setting standards for quality, clarity, scientific integrity and credibility across all communications.
• Creation and delivery of the medical content required to deliver the medical comms strategy.

Requirements

• Degree (or equivalent experience) in a life sciences discipline.
• Strong experience in medical communications, medical writing, or scientific content development (pharma, biotech, or agency).
• Strong ability and experience to differentiate between promotional and non-promotional content and support the compliant development for both as relevant.
• Proven ability to translate complex scientific data into clear, engaging, and commercially relevant communications.
• Excellent writing, editing, and proofreading skills.
• Experience working across both medical and commercial teams, with an understanding of how to balance scientific integrity with business impact.
• Experience supporting both medical and commercial initiatives (e.g. events, campaigns, publications).
• Strong organisational skills with the ability to manage multiple projects end-to-end.
• Collaborative mindset with the ability to work across cross-functional teams and build strong internal and external relationships.
• Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook).

Preferred

• Experience as reviewer/content owner in Medical, Legal and Regulatory review processes and compliance to US FDA OPDP regulations and guidelines.
• Experience in a regulated industry (pharma/biotech/healthcare).
• Familiarity with content approval processes and compliance requirements (e.g. Veeva PromoMats).
• Experience working with digital channels and content delivery platforms.

Benefits

• A collaborative high performing work environment
• Performance based bonus
• Hybrid working with flexible start and finish times
• Opportunity to join a fast growing and ambitious business
• Company pension scheme
• 100% employer paid membership for Private Health Insurance
• Life and Critical Illness Insurance
• Corporate Gym membership
• Regular team building events and an agile working environment