Medical Content Development Manager – Team Lead

🔥 0 minutes ago

🇮🇹 Italy – Remote

⏰ Full Time

🟠 Senior

👨🏼‍💻 Content Manager

👻 Ghost score 10%

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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 and management engagements • Write and create medical and scientific content for Medical Affairs, Medical Information, and Medical Communications, including SRDs, FAQs, slide sets, abstracts, posters, and education/training materials • Drive client document development from gathering source materials through scientifically rigorous content development and MLR review meetings • Use EVERSANA or client document management platforms such as Veeva PromoMats / MedComms; upload documents and provide reference anchoring and annotations • Perform scientific data fact-checking to support medical reviewers on MLR teams • Collaborate on strategy, tactical execution, and communication approaches for assigned projects • Direct and work with medical writers and medical content development teams to deliver client projects efficiently • 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 technologies and procedures improving operational efficiency and material quality • Collaborate with medical writers and creative teams across EVERSANA • Demonstrate commitment to diversity, equity, and inclusion • Deliver client delight, maintain compliance with industry standards and codes of practice, and independently produce accurate, ethical, compliant, strategically aligned medical content • Proactively identify and manage quality issues and ensure timely corrective and preventive actions • Work full time with scheduling flexibility based on client and management needs; travel 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 with a Medical Information / Medical Communications service provider • Experience developing global medical information materials, including SRDs, FAQs, and CRDs • Exceptional written, oral, interpersonal, and presentation skills • Ability to independently interpret and summarize complex results • Ability to establish credibility with clients and effectively interface 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/non-promotional materials review • Excellent project management skills and a results-driven track record • Ability to conceptualize, design, and deliver best-in-class solutions • Fluent English, written and verbal • One or more additional European languages at CEFR level B2, C1, or C2 • Ability to analyze, digest, and interpret complex scientific information and data • Ability to develop and execute project plans independently and with clients and cross-functional teams • Ability to manage, coordinate, and oversee assigned client relationships and projects • Valid work permit in the European Union or the United Kingdom • Preferred: Pharm.D., Pharm.M., Medicine degree, PhD, or relevant Bachelor’s Degree in Life Science • Preferred experience across multiple therapeutic areas and with new product launches and current-material updates

🏖️ Benefits

• Remote/home-office-based work • Full-time employment • Business travel opportunities (approximately 10–15%) • Diversity, equity, and inclusion commitment • Professional development and investment in employee development • Equal opportunity employment