Full-Time Medical Content Development Manager

Medical Information is a critically important customer-facing function. It supports the safe and effective use of pharmaceutical, biopharmaceutical, medical device, and digital therapeutic products by providing timely, scientifically balanced, evidence-based, non-promotional information in response to unsolicited requests.

This role is responsible for medical content development-related client engagements. This requires medical information and medical content experience and knowledge, excellent communication skills (both verbal and written). Must be legally eligible to work in the European Union / United Kingdom.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Plays a key role supporting the Global Medical Information/Medical Content Development Team on content development for clients.
• Writes and creates medical and scientific content (e.g., Scientific Response Documents (SRDs), Frequently Asked Question (FAQ) documents, Slide Sets, Abstracts, Posters, Education and Training materials).
• Drives the client document development process from material gathering to MLR review meetings.
• Works with document management platforms (e.g., Veeva PromoMats/MedComms).
• May perform scientific data fact-checking.
• Collaborates with the team and contributes to discussions on strategy and execution.
• Provides direction to medical writers.
• Participates in client meetings.
• Supports creation/updating of SOPs, checklists, templates, style guides, and guidance documents.
• Stays knowledgeable of industry best practices and supports leadership in evaluating and implementing new technologies.
• Works collaboratively with other medical writers and creative teams.
• Performs other duties as assigned.

MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:

• Doctorate or Master's degree in Life Sciences or healthcare or equivalent.
• 2+ years experience in pharmaceutical industry or Medical Information/Medical Communications service provider.
• Experience developing global medical information materials (e.g., SRDs, FAQs, CRDs).
• Exceptional written, oral, interpersonal, and presentation skills.
• Strong editing and Microsoft Office skills.
• Experience conducting literature searches and using tools like PubMed, Ovid, Embase.
• Experience with reference management software (e.g., EndNote).
• Understanding of regulatory requirements and best practices.
• Strong project management skills and a results-driven approach.

PREFERRED QUALIFICATIONS:

• Pharm.D., Pharm.M, or Medical Degree is preferred.
• Experience with multiple therapeutic areas.
• Fluency in English and one or more other European languages.

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