Job Description

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

Salary: Commensurate with experience

Full-Time - Monday through Friday - 9:00 am to 5:00 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 skilled and detail-oriented Medical Writer to develop high-quality, scientifically grounded content across promotional and non-promotional medical communications. The ideal candidate combines scientific expertise with strong writing and collaboration skills, ensuring every deliverable is accurate, referenced, compliant, and strategically aligned with client objectives.

Please be prepared to participate in a structured writing task/test.

Responsibilities

• Develop clear, engaging, and scientifically accurate content for a range of deliverables, including needs assessments, advisory board materials, executive summaries, publications, websites, and promotional assets.
• Conduct literature reviews and ensure content is fully referenced, annotated, and compliant with client and regulatory standards.
• Revise and refine content based on internal and client feedback to maintain accuracy, clarity, and alignment with brand and scientific strategy.
• Partner with medical and client teams to present materials during content review calls and facilitate communication with clients and KOLs.
• Manage organization, version control, and documentation of content and references across shared platforms.
• Prepare materials for MLR submission, maintain required certifications, and support live review calls.
• Collaborate with project management to meet deadlines and maintain consistency across deliverables.
• Participate in quarterly travel for internal team sessions, with additional travel as needed for key client events or engagements.

Qualifications

• Master’s degree in a scientific discipline required; doctorate (PhD, PharmD, MD) preferred.
• Minimum 2 years of experience in medical communications or related scientific writing.
• Proven ability to translate complex data into clear, accurate, and engaging content.
• Familiarity with MLR processes and promotional medical content standards and regulations.
• Proficiency in Microsoft Office, Adobe Acrobat, and reference management tools.
• Exceptional attention to detail, organization, and time management.
• Strong communication skills and ability to work both independently and collaboratively in a fast-paced environment.

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