Medical Content Development Manager – Team Lead

🔥 1 hour ago

🇮🇹 Italy – Remote

⏰ Full Time

🟠 Senior

👨🏼‍💻 Content Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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EVERSANA

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

💼 Consulting

🏥 Healthcare

⚕️ Healthcare Insurance

Consulting • Healthcare • Healthcare Insurance

EVERSANA is a comprehensive service provider focused on integrated commercial solutions for the life sciences industry. The company offers a wide range of services including advisory and management consulting, regulatory consulting, patient services, market access strategies, pricing and revenue management, medical affairs, and digital transformation. EVERSANA is known for its expertise in drug commercialization, enabling companies to effectively launch and manage pharmaceutical products. With a platform powered by data and analytics, EVERSANA addresses challenges related to drug pricing, market access, patient adherence, and product delivery, helping companies optimize their commercial strategies and enhance patient outcomes. The company emphasizes innovation and has been recognized for its use of AI and data analytics within the life sciences sector.

📋 Description

• Support the Global Medical Information / Medical Content Development Team on client medical content development engagements • Write and create medical and scientific content for Medical Affairs, Medical Information, and Medical Communications • Develop scientific response documents, FAQ documents, slide sets, abstracts, posters, education and training materials, and related content • Drive document development from gathering materials and creating scientifically rigorous content through medical, legal, and regulatory review meetings • Manage documents in EVERSANA and client document management platforms such as Veeva PromoMats and MedComms • Upload documents and provide reference anchoring and annotations as required • Perform scientific data fact checking to support medical reviewers • Collaborate on strategy, tactical execution, and communication approaches for assigned projects • Provide direction to medical writers and medical content development team members • Participate in assigned client meetings • Create and update SOPs, checklists, templates, style guides, and guidance documents • Stay current with industry best practices and support evaluation and implementation of new technologies and procedures • Collaborate with medical writers and creative teams across EVERSANA • Deliver high-quality, scientifically accurate, strategically aligned, ethical, and compliant medical content • Proactively identify quality issues and manage timely corrective and preventive actions • Travel for business approximately 10–15% as required

🎯 Requirements

• Doctorate or Master of Science (MSc) degree in Life Sciences or healthcare or equivalent • Minimum 2 years of experience in the pharmaceutical industry or as a Medical Information / Medical Communications service provider • Experience developing global medical information materials, including scientific response documents, FAQs, and custom response documents • Excellent written, verbal, interpersonal, and presentation skills • Ability to independently interpret and summarize complex results • Ability to establish credibility with clients and interface effectively with all levels of management and staff • Ability to work successfully in a matrix team setting while meeting or exceeding timelines • Proficient editing skills and expertise in Microsoft Office, Acrobat, and other applications • Experience conducting literature searches using PubMed, Ovid, Embase, or similar tools • Experience with reference management and citation software such as EndNote, Mendeley, or Citavi • Strong understanding of regulatory requirements and best practices for Medical Information, Medical Affairs, and promotional and non-promotional materials review • Excellent project management skills and a proven results-driven track record • Ability to conceptualize, design, and deliver best-in-class solutions • Valid work permit in the European Union or the UK • Able to work full time and maintain flexible scheduling as required by clients and management • Fluent in English, written and verbal, plus one or more other European language at CEFR level B2, C1, or C2 • Pharm.D., Pharm.M., Medicine degree, or PhD preferred; relevant Bachelor’s Degree in a Life Science also considered • Ability to analyze, digest, and interpret complex scientific information and data • Ability to develop project plans and execute them independently and with clients and cross-functional teams • Ability to manage, coordinate, and oversee assigned client relationships and projects

🏖️ Benefits

• Great Place to Work certification • Remote/home office-based work • Diversity, equity, and inclusion-focused culture • Opportunity to work with global teams and clients • Professional development through continuous development and talent investment • Business travel opportunities