Principal Medical Affairs Specialist, Scientific Communications at Diabetes Youth Families | Hybrid Hired

About the role

Lead a portfolio of complex, high-impact scientific communications projects with minimal oversight, ensuring alignment with global publication strategy and business objectives.
Contribute expert input to publication planning discussions, and serve as a senior resource for resolving scientific or editorial challenges in publications.
Author, review, and approve complex scientific documents (e.g., manuscripts, white papers, abstracts, congress presentations) that clearly communicate clinical study results and product value for diverse audiences.
Interpret complex clinical data and lead the design of innovative data visualizations to maximize clarity and impact.
Drive publication review cycles, integrating feedback from authors, investigators, internal stakeholders, and peer-reviewers with strategic insight.
Partner with statisticians and data scientists to propose novel data analyses that support publication objectives and are aligned with the global integrated evidence plan.
Provide scientific oversight for publications resulting from investigator-initiated studies and collaborative research projects with external partners.
Serve as a consultant to cross-functional teams (Clinical, Regulatory, Commercial, R&D), providing expert guidance on the interpretation and use of clinical data.
Mentor and provide scientific oversight to junior writers and team members, fostering professional growth and knowledge sharing.
Build and maintain relationships with external investigators, professional societies, and publication venues to enhance Insulet’s scientific reputation.
Continuously improve scientific writing processes, templates, and standards to enhance quality and efficiency.
Set standards for scientific writing quality, data integrity, and compliance with industry guidelines (GPP, ICMJE, company policies).

Requirements

An advanced degree (PhD, PharmD, MD, or equivalent) in life sciences, public health, or a related field
8-10 years of related experience in clinical research, medical writing, and scientific communications within the medical device or pharmaceutical industry
Expert-level knowledge of the medical publications process, including peer-reviewed submissions, congress presentations, and publication planning
Deep clinical or scientific expertise in diabetes disease state and diabetes technologies (e.g., insulin pumps, continuous glucose monitors)
Strong understanding of clinical trial design, biostatistics, and regulatory requirements.
Demonstrated ability to translate complex clinical data into compelling narratives for diverse audiences.
Advanced proficiency in Microsoft Office, reference management tools (e.g., EndNote), and data visualization platforms (e.g., GraphPad Prism).
Strong understanding of publication ethics, regulatory standards, and healthcare compliance frameworks.

Benefits

Medical, dental, and vision insurance
401(k) with company match
Paid time off (PTO)
And additional employee wellness programs

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