Medical Content Development Manager – Team Lead

🔥 0 minutes ago

🇪🇸 Spain – 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 • Develop scientific response documents, FAQ documents, slide sets, abstracts, posters, education and training materials, and related content • Drive the client document development process from gathering source materials through scientifically rigorous content development • Facilitate document review and discussions at medical, legal, and regulatory review meetings • Manage documents in EVERSANA or 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 on MLR teams • Collaborate with the Global Medical Information / Medical Content Development Team on strategy, tactical execution, and communication approaches • Direct and work closely with medical writers and medical content development team members to deliver client projects efficiently • Participate in assigned client meetings • Create and update SOPs, checklists, templates, style guides, and guidance documents • Monitor industry best practices and support evaluation and implementation of technologies and procedures to improve operational efficiency and material quality • Collaborate with medical writers and creative teams across EVERSANA • Deliver client delight, maintain compliance with industry standards and codes of practice, and ensure high-quality, scientifically accurate, strategically aligned, ethical, and compliant medical content • Proactively identify quality issues and manage timely corrective and preventive actions

🎯 Requirements

• Doctorate or Master of Science (MSc) degree in Life Sciences or healthcare or equivalent • Minimum of 2 years of experience in the pharmaceutical industry or with a Medical Information / Medical Communications service provider • Experience developing global medical information materials, including scientific response documents, frequently asked questions, and custom response documents • Excellent written, oral, interpersonal, and presentation skills • Ability to independently interpret and summarize complex results • Ability to establish credibility with clients and diverse audiences • Ability to interface effectively with all levels of management and staff 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 • Must hold a 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 • Preferred: Pharm.D., Pharm.M., Medicine degree, or PhD • Preferred: Relevant Bachelor’s Degree in a Life Science • Fluent in English, written and verbal, plus one or more European languages at CEFR B2, C1, or C2 level • Ability to analyze, digest, and interpret complex scientific information and data • Ability to develop project plans and execute them independently and collaboratively • Ability to manage, coordinate, and oversee assigned client relationships and projects

🏖️ Benefits

• Home office-based full-time position • Opportunity to work remotely • Business travel of approximately 10–15% as required • Diversity, equity, and inclusion-focused workplace • Professional development and investment in employee development • Equal opportunity employment