Medical Content Development Specialist

November 13

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EVERSANA

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Healthcare Insurance • Pharmaceuticals

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.

5001 - 10000 employees

⚕️ Healthcare Insurance

💊 Pharmaceuticals

📋 Description

• Plays an essential role supporting Manager, Medical Content Development on content development-related engagements for integrated and complete commercialization deals as well as for clients who require medical information or medical affairs consulting services outside of EVERSANA’s complete commercialization partnerships. • Writes and creates medical and scientific content related to Medical Affairs, Medical Information and Medical Communications including, but not limited to, Scientific Response Documents (SRD), Frequently Asked Question (FAQ) documents, Slide Sets, Abstracts, Posters, Education and Training materials, and others for potential clients. • Drives the client document development process from gathering materials and developing scientifically rigorous content to facilitating document review and discussions at medical, legal, regulatory (MLR) review meetings. • Works with EVERSANA and/or client-provided document management technology platforms (i.e., Veeva PromoMats / MedComms, etc.) as content owner when appropriate, uploading documents, providing reference anchoring and annotations as required. • Supports creating/updating the SOPs, checklists, templates, style guides, and guidance documents as necessary.

🎯 Requirements

• Doctorate or Master of Science (MSc) degree in Life Sciences or healthcare or equivalent. • A minimum of 2-year(s) experience in pharmaceutical industry or Medical Information / Medical Communications service provider. • Experience developing global medical information materials, e.g., scientific response documents (SRDs), frequently asked questions (FAQs), custom response documents (CRDs), etc. • Exceptional written, oral, interpersonal, and presentation skills including the ability to independently interpret and summarize complex results. • Ability to establish credibility with a variety of audiences; especially with clients • Ability to effectively interface with all levels of management and staff and to succeed in a matrix team setting while meeting or exceeding timelines. • Proficient editing skills along with expertise in Microsoft Office, Acrobat and other applications. • Experience conducting literature searches and working with tools such as PubMed, Ovid, Embase, etc. • Strong understanding of regulatory requirements and best practices in relationship to Medical Information, Medical Affairs and promotional and non-promotional materials review • Excellent project management skills and proven track record of being results driven

🏖️ Benefits

• Flexible working hours • Professional development opportunities