HMP Global

Location: Remote or Hybrid (East Windsor, NJ or Malvern, PA) 3 days in-office/2 days work-from-home, dependent upon your location

Salary: Commensurate with experience

Full-Time - Monday through Friday - 8:30 am to 4:30 pm

Strong Benefits Package (Medical, Dental, Vision, 401k w/company match)

Discretionary bonus eligible

HMP Global is a leading healthcare event and education company, holding a dominant position in several therapeutic areas, including Oncology, psychiatry and behavioral health, Cardiovascular, Wound Care, and Public Safety. With a mission to improve patient care, we deliver information and education to healthcare professionals through over 400 global, regional, and local events, reaching more than 2 million users monthly through digital networks and social channels.

HMP Collective is seeking a highly skilled Medical Writer with deep expertise in medical content development across promotional and non-promotional communications. This role is ideal for a content development expert who can independently build high-quality, scientifically rigorous materials and establish and reinforce best practices in medical communications. The ideal candidate is an exceptional writer with strong scientific judgment, advanced content refinement skills, and hands-on proficiency in Veeva Vault.

Please be prepared to participate in a structured writing task.

Responsibilities

• Lead development of clear, compelling, scientifically rigorous content across a range of medical communications deliverables.
• Serve as an internal content development expert, elevating the scientific quality, strategic coherence, and consistency of materials across projects.
• Translate complex clinical and scientific data into accurate, audience-appropriate content that tells a clear scientific story and supports the intended communication objective.
• Conduct literature review, source evaluation, referencing, annotation, and fact verification to ensure all content is evidence-based, fully substantiated, and compliant.
• Review, revise, and refine draft content based on stakeholder feedback while preserving scientific accuracy, clarity, and strategic intent.
• Establish, model, and reinforce good medical communications practice, including content standards, annotation quality, review readiness, and document quality control.
• Prepare, route, and maintain materials in Veeva Vault, including version control, documentation, and support for review/approval.
• Partner closely with internal strategy, editorial, and project management colleagues to deliver high-quality work on time and with consistency across deliverables.

Qualifications

• Master’s degree in a scientific discipline required; doctorate (PhD, PharmD, MD) preferred.
• Minimum 3 years of experience in medical communications, scientific writing, or promotional/non-promotional content development required.
• Demonstrated proficiency in Veeva Vault required.
• Strong command of medical editing, referencing, annotation, fact-checking, and quality review standards.
• Strong familiarity with MLR processes, promotional review standards, and content development workflows.
• Exceptional attention to detail, organization, judgment, and independent ownership of content quality.
• Strong internal collaboration skills.

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