Medical Content Development Manager – Team Lead

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Assist the Global Medical Information / Medical Content Development Team with client-focused medical content development and management projects.

• Craft and produce medical and scientific content for Medical Affairs, Medical Information, and Medical Communications, encompassing SRDs, FAQs, slide presentations, abstracts, posters, as well as educational and training resources.

• Lead the development of client documents by sourcing materials and creating scientifically robust content through MLR review sessions.

• Utilize document management systems such as Veeva PromoMats / MedComms as the content owner, including the uploading of documents, reference anchoring, and making annotations.

• Conduct scientific data verification to assist medical reviewers on MLR teams.

• Collaborate on strategy, tactical implementation, and communication methods for designated projects.

• Directly engage with medical writers and medical content development teams to ensure the timely and effective delivery of client projects.

• Take part in crucial client meetings.

• Develop and revise SOPs, checklists, templates, style guides, and other guidance documents.

• Assess and adopt new technologies and processes to enhance operational efficiency and quality of materials.

• Work in collaboration with medical writers and creative teams within EVERSANA.

• Ensure client satisfaction while adhering to industry standards and codes of conduct.

• Independently produce high-quality, scientifically accurate, strategically aligned, ethical, and compliant medical content.

• Actively identify and manage quality concerns and ensure prompt corrective and preventive measures.

⛳️ Requirements

• Doctorate or Master of Science (MSc) degree in Life Sciences, healthcare, or a related field.

• At least 2 years of experience in the pharmaceutical sector or with a Medical Information / Medical Communications service provider.

• Proven experience in developing global medical information materials, including SRDs, FAQs, and CRDs.

• Outstanding written, verbal, interpersonal, and presentation skills.

• Ability to independently analyze and summarize complex findings.

• Capability to establish credibility with clients and effectively interact with all levels of management and staff in a matrix team environment.

• Strong editing skills and proficiency in Microsoft Office, Acrobat, and other relevant applications.

• Experience conducting literature searches using platforms such as PubMed, Ovid, Embase, or similar resources.

• Familiarity with reference management and citation software like EndNote, Mendeley, or Citavi.

• Solid understanding of regulatory requirements and best practices pertaining to Medical Information, Medical Affairs, and the review of promotional and non-promotional materials.

• Excellent project management abilities and a proven track record of results.

• Ability to conceptualize, design, and provide top-tier solutions.

• Must possess a valid work permit in the European Union or the UK.

• Fluent in English, both written and spoken.

• Proficiency in one or more additional European languages at Common European Framework levels B2, C1, or C2.

• Preferred qualifications include a Pharm.D., Pharm.M., Medicine degree, or PhD.

• A relevant Bachelor's Degree in a Life Science will also be considered.

• Experience in Medical Information, Medical Communications, Medical Writing, or Medical Affairs.

• Experience in developing medical content for new product launches and managing existing materials.

• Background across multiple therapeutic areas.

🏝️ Benefits

• Full-time remote work opportunity.

• Opportunities for business travel (approximately 10–15%).

• Equal Opportunity Employer.

• Inclusive culture that emphasizes diversity, equity, and inclusion.

• Commitment to employee development and investment in the growth of others.