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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