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EVERSANA is a global commercialization services company serving the life sciences industry, with 7,000+ employees and 650+ clients ranging from biotech startups to established pharmaceutical companies. The company provides next-generation services to help bring innovative therapies to market and support patients.
This Medical Content Development Manager role is a team lead position within the Global Medical Information / Medical Content Development Team. The role is home office-based (full-time) and requires a valid work permit in the EU or UK.
KEY RESPONSIBILITIES:
- Lead and provide direction to medical writers and medical content development team members to deliver client projects efficiently and effectively
- Develop and manage medical and scientific content including Scientific Response Documents (SRDs), Frequently Asked Questions (FAQs), slide sets, abstracts, posters, education and training materials
- Drive the client document development process from gathering materials through facilitating Medical, Legal, Regulatory (MLR) review meetings
- Manage document development using platforms such as Veeva PromoMats / MedComms, uploading documents and providing reference anchoring
- Conduct scientific data fact-checking for documents in support of medical reviewers
- Collaborate with Global Medical Information / Medical Content Development Team on strategy, tactical execution, and communication approaches
- Participate in key client meetings as assigned
- Support creation and updates of SOPs, checklists, templates, style guides, and guidance documents
- Stay current with industry best practices and evaluate new technologies to improve operational efficiency
- Work collaboratively across EVERSANA teams including medical writers and creative teams
- Ensure compliance with industry standards and codes of practice
- Manage quality issues proactively with timely corrective and preventive actions
- Travel up to 10-15% as required
- Flexible scheduling to meet client and management needs
REQUIREMENTS:
Minimum Education: Doctorate or Master of Science (MSc) degree in Life Sciences or healthcare, or equivalent.
Minimum Experience:
- Minimum 2 years in pharmaceutical industry or Medical Information / Medical Communications service provider
- Experience developing global medical information materials (SRDs, FAQs, CRDs, etc.)
- Exceptional written, verbal, interpersonal, and presentation skills with ability to independently interpret and summarize complex results
- Ability to establish credibility with diverse audiences, especially clients
- Effective interface with all management levels in matrix team settings while meeting timelines
- Proficient editing skills and expertise in Microsoft Office, Acrobat, and related applications
- Experience conducting literature searches using PubMed, Ovid, Embase, etc.
- Experience with reference management and citation software (EndNote, Mendeley, Citavi, etc.)
- Strong understanding of regulatory requirements and best practices in Medical Information, Medical Affairs, and promotional/non-promotional materials review
- Excellent project management skills with proven results-driven track record
- Ability to conceptualize, design, and deliver best-in-class solutions
Preferred Qualifications:
- Pharm.D., Pharm.M., Medicine degree, or PhD
- Relevant Bachelor's degree in Life Sciences
- Medical Information, Medical Communications, Medical Writing, or Medical Affairs experience
- Experience developing medical content for new product launches and managing current materials across multiple therapeutic areas
- Fluent in English (written and verbal) plus one or more additional European language at B2, C1, or C2 level on Common European Framework
- Strong analytical and critical thinking abilities
- Proven ability to develop and execute project plans
- Track record of delivering results
- Demonstrated innovation and integrity
- Client management and coordination experience
