Fully remote - UK based 4 months contract - Umbrella (2-3 days per week) £up to 650 per day Immediate start Are you exploring new career paths? We have an exciting opportunity for those seeking a change from full-time roles in larger companies. We are in search of a dedicated Medical Affairs contractor with several years of experience to join our clients committed team on a part-time basis (2-3 days per week). This role presents various chances to contribute to our goal of improving patient outcomes. The Medical Affairs Contractor will provide medical review oversight and support for two products in partnership with the Clinical and Scientific Advisor (CSA). This contractor will ensure materials are scientifically accurate, compliant, and aligned with regulatory standards, while assisting with speaker/KOL development. KEY RESPONSIBILITIES: Product 1: Internal Materials & Training Oversee the CSA’s data analysis and evidence-gathering to ensure accuracy and compliance. Review newly created or revised training materials (produced by the CSA or internal teams) for scientific correctness. Offer guidance on the most up-to-date product information and best practices for training. External Promotional Materials Collaborate with the CSA and Marketing to review promotional claims and materials (e.g., brochures, digital content). Ensure any external-facing content is consistent, evidence-based, and meets regulatory standards. Provide final oversight (but not signatory approval) to confirm compliance before materials are released. Speakers & Webinars Support the identification and development of speakers/KOLs for snK. Participate in content discussions to shape speaker decks (originally created by the CSA), ensuring data accuracy. Provide guidance on webinar material creation and host or co-host if needed, focusing on the scientific narrative. Product 2: Medical Information (MI) Oversight Coordinate with the CSA on MI responses, ensuring they are clinically sound and up to date. Provide a secondary review layer (oversight only) to confirm the scientific appropriateness of interim responses. Data Presentations Review and refine data decks (compiled by the CSA) for MV140, ensuring accuracy and consistency with recent evidence. Work with internal or external stakeholders to finalize presentation content, verifying compliance. Additional Responsibilities Medical Review of Materials: Serve as a trusted reviewer for internal and external documents, promotional or otherwise, originating from the CSA or cross-functional teams. Speaker/KOL Engagement: Collaborate on speaker selection and provide scientific insights to ensure messaging is accurate and relevant. Cross-Functional Collaboration: Work closely with Marketing, Regulatory, and Sales/Distributors to align on product messaging and ensure all materials meet regulatory standards. Regulatory & Compliance Alignment: Remain vigilant about local regulations and guidelines, providing oversight but not acting as final signatory. QUALIFICATIONS & EXPERIENCE: Advanced degree (PharmD, MD, PhD, or MSc in life sciences) preferred. At least 3 years of experience in Medical Affairs (or a related scientific role) within the pharmaceutical/biotech industry. Strong understanding of regulatory requirements and medical review processes for promotional and non-promotional content. Excellent communication skills and experience working with cross-functional teams (Marketing, Regulatory, Medical, etc.). Experience with speaker and KOL engagement is highly desirable. Should you not hear back from Projectus Consulting within 7 days of your application please assume you have not been selected on this occasion only.