Medical Content Development Manager/Project Lead

Responsibilities

• Write and create medical and scientific content including Scientific Response Documents (SRD), FAQs, Slide Sets, and training materials
• Drive the client document development process from material gathering to medical, legal, and regulatory (MLR) review
• Manage content within document management platforms like Veeva Promo Mats
• Perform scientific data fact-checking for medical reviewers
• Collaborate with the Global Medical Information team on strategy and tactical execution
• Provide direction to other medical writers to ensure efficient project delivery
• Support the creation and updating of SOPs, checklists, and style guides

Requirements

• Doctorate or Master of Science (MSc) in Life Sciences or healthcare (Bachelor's in Life Science considered)
• Minimum 2 years of experience in the pharmaceutical industry or Medical Information/Communications
• Experience developing global medical information materials (SRDs, FAQs, etc.)
• Proficiency in Microsoft Office, Acrobat, and literature search tools (PubMed, Ovid, Embase)
• Experience with reference management software (EndNote, Mendeley, etc.)
• Strong understanding of regulatory requirements for Medical Affairs and promotional/non-promotional materials
• Excellent project management and communication skills

Preferred Qualifications

• Pharm.D., MD, or PhD degree
• Experience with new product launches and managing materials across multiple therapeutic areas
• Proven ability to manage client relationships and oversee complex projects

About the Company

EVERSANA is a global commercialization services provider for the life sciences industry, helping bring innovative therapies to market and supporting patients through next-generation solutions.