Senior Medical Communications Writer - Medical Affairs, North America

Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need.

Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.

As a Senior Medical Communications Writer on the Medical Affairs, North America team, you will be responsible for researching, writing, and editing scientific publications and communications materials that advance the understanding of rare MC4R pathway diseases and support Rhythm’s medical communications objectives. You will serve as a key contributor to manuscript development, congress activities, publication project management, and scientific communications initiatives, partnering closely with Medical Affairs North America, Global Scientific Communications, Value & Evidence and other cross-functional partners, as well as external authors.

• Draft, edit, and coordinate development of manuscripts, abstracts, posters, review articles, proceedings papers, case reports, and scientific presentations
• Help manage publication projects from concept through publication, ensuring adherence to timelines, quality standards, and publication best practices
• Support congress planning and execution including abstract submissions, poster development, oral presentations, and other publication-related activities
• Participate in publication planning activities and support implementation of publication strategy and evidence dissemination plans
• Collaborate with cross functional partners to ensure scientific alignment and effective dissemination of evidence
• Ensure compliance with Good Publication Practice (GPP), ICMJE recommendations, company policies, and applicable industry standards

• BS/BA in scientific discipline preferred, advanced degree is a plus
• 6+ years of related experience, across any combination of key focus areas: medical publications, medical affairs and project management, with at least 2 years focused on publications in a pharmaceutical/biotech environment
• Experience in obesity or rare diseases is preferred
• Proven scientific writing skills, particularly experience with developing scientific peer-reviewed publications
• Understanding of drug development, clinical research, study design, biostatistics, pharmacology, and medical terminology
• Exceptional collaboration, written, and verbal communication skills. Comfortable partnering with co-authors (both internally with Global Scientific Communications and Clinical Operations teams and externally with HCPs)
• Ability to independently resolve document content issues and address questions by resolving discrepancies
• Proficiency with literature databases, reference management tools (e.g., End Note), Microsoft Office, and publication management systems (e.g., iEnvision)
• Strong project management and organizational skills
• Strong attention to detail and commitment to scientific quality and accuracy
• Ability to work independently, prioritize, and multitask within a highly dynamic environment to meet timelines under evolving conditions
• High learning agility, adaptable to change and proactive in identifying opportunities to create and enhance existing programs and processes

This role is based out of our corporate…