Manager Medical Communication

The Manager of Medical Communications will be responsible for developing and maintaining high quality scientific and medical materials that support healthcare provider (HCP) engagement, product understanding, and safe and effective use of Sequel products.   

The Manager will own the creation and maintenance of standard response letters, HCP-facing scientific materials, and scientific slide decks. They will manage Sequel's publication roadmap,  including planning, prioritization, and stakeholder alignment, and serve as a primary author/medical writer for abstracts, posters, manuscripts, and congress content. This individual will collaborate closely with Medical, Regulatory, Legal, and external partners to ensure accuracy, compliance, and consistency across all scientific communications.  

This role is ideal for a PharmD or advanced scientific professional with strong writing ability and experience in medical information, publications, and scientific communication. 

• Education: PharmD strongly preferred; alternatively, PhD, MD, MS, or equivalent advanced scientific degree with demonstrated expertise in medical communications within healthcare technology.   

• Experience: 3+ years of experience in medical communications or medical information within a medical device, digital health, or MedTech company, ideally supporting FDA regulated products  

• Experience working in diabetes, metabolic disease, endocrinology, or automated insulin delivery (AID) systems; either through prior roles, fellowship training, publications, or direct industry exposure. 

• Proven ability to interpret clinical data relevant to diabetes care, including CGM, pump therapy, AID algorithms, and real‑world evidence, and translate this into scientifically accurate materials.   

• Comfort with TIR/TBR/GMI metrics, paired analyses, and basic interpretation of propensity-matched RWE 

• Demonstrated experience developing HCP‑facing scientific resources, standard response letters, or medical information content in an environment with structured Medical Materials review processes (Medical/Legal/Regulatory).   

• Proficiency in medical device labeling rules, scientific exchange standards, and appropriate management of on and off-label communication for FDA regulations. 

• Strong capability in creating scientific slide decks and data driven presentations for internal and external audiences. 

• Demonstrated track record of personally authoring peer-reviewed publications (first or contributing author on abstracts, posters, and manuscripts) in addition to managing publication plans including congress submissions and scientific narratives 

• Ability to work cross-functionally with clinicians, engineers, regulatory affairs, quality, marketing, and external collaborators typical of medtech organizations 

• Exceptional written communication skills with meticulous attention to scientific accuracy and regulatory compliance.   

• Comfortable working in a rapid iteration, innovation focused medtech environment where systems evolve quickly and evidence generation is ongoing.