Medical Content Development Manager / Project Lead

Medical Information role supporting the development and management of medical content for pharmaceutical, biopharmaceutical, medical device, and digital therapeutic products. The position involves creating scientifically rigorous content, supporting client engagements, and ensuring compliance with industry standards.

Location: Remote (US)

Salary: $100k–$120k

Responsibilities

• Support Global Medical Information / Medical Content Development Team on content development-related engagements.
• Write and create medical and scientific content including Scientific Response Documents (SRD), FAQs, Slide Sets, Abstracts, Posters, Education and Training materials.
• Drive the client document development process from gathering materials to facilitating review meetings.
• Work with document management platforms such as Veeva Promo Mats / Med Comms.
• Perform scientific data fact checking for documents.
• Collaborate with teams on strategy, execution, and communication for projects.
• Provide direction to medical writers and content development team.
• Participate in client meetings.
• Support creation and updating of SOPs, checklists, templates, and style guides.
• Stay knowledgeable of industry best practices and support technology implementation.
• Work collaboratively across teams.
• Demonstrate commitment to diversity, equity, and inclusion.
• Perform other duties as assigned.

Requirements

• Doctorate or Master of Science (MSc) in Life Sciences or healthcare, or relevant bachelor’s degree.
• Minimum 2 years of experience in pharmaceutical industry or Medical Information / Medical Communications.
• Experience developing global medical information materials.
• Excellent written, oral, interpersonal, and presentation skills.
• Ability to interpret and summarize complex results.
• Proficient in Microsoft Office, Acrobat, and other applications.
• Experience with literature searches and tools like PubMed, Ovid, Embase.
• Experience with reference management software (EndNote, Mendeley, Citavi).
• Strong understanding of regulatory requirements in Medical Information and Medical Affairs.
• Excellent project management skills.