Publications Science Director, Endocrinology

Vertex Pharmaceuticals•Boston, MA

7d•Hybrid

About The Position

Vertex is seeking an accomplished scientific communications leader to serve as Publications Science Director, Medical Affairs (Endocrinology). Following the Crinetics acquisition, this role will lead the global publications strategy, planning, development, and execution for Vertex’s rare endocrinology portfolio, including the commercialized acromegaly franchise and the pipeline program in congenital adrenal hyperplasia (CAH), with the flexibility to support future endocrinology indications as the portfolio evolves. Working closely with the Global Medical Lead (GML), the Science Director will translate scientific and medical priorities into an integrated publication strategy that communicates clinically meaningful evidence to healthcare professionals and the broader endocrine and rare disease communities. The role will connect evidence gaps, clinical and real-world data, scientific literature, treatment guidelines, medical insights, and the external landscape to ensure publications are scientifically rigorous, medically accurate, balanced, timely, and aligned with the global medical plan. This role may also support the development of medical content and scientific materials, including slide decks, FAQs, congress materials, and other external-facing resources. The Science Director will partner closely with Global and Regional Medical, Research, Development, Biostatistics, Health Economics and Outcomes Research (HEOR), Real-World Evidence (RWE), Regulatory, Legal, Compliance, and Commercial colleagues. The role reports to the disease area GML and serves as a core member of the Endocrinology Global Medical team.

Requirements

Advanced scientific or medical degree, such as an MS, PharmD, PhD, MD, or equivalent relevant experience.
Typically requires 10 years of relevant experience, or the equivalent combination of education and experience, including 3 or more years in Medical Affairs, clinical development, publications, or scientific communications.
Demonstrated experience developing and executing global publication strategies and plans within the pharmaceutical, biotechnology, academic medicine, or related environment.
Experience leading cross-functional publication teams and managing external authors, investigators, and agency partners in a highly matrixed, global organization.
Demonstrated experience interpreting and communicating clinical trial data, real-world evidence, published literature, and other scientific evidence.
Working knowledge of publication standards, authorship principles, and relevant regulatory, legal, compliance, and data privacy requirements governing scientific exchange and publication activities.

Nice To Haves

Rare disease, specialty medicine, or endocrinology experience is strongly preferred; experience in acromegaly, congenital adrenal hyperplasia (CAH), or related endocrine conditions is a plus.
Experience working across both global and country or regional Medical Affairs organizations is desired.

Responsibilities

Develop and execute the integrated global publication strategy and plans for the rare endocrinology portfolio, including acromegaly and CAH, as part of the annual global medical planning process and in partnership with the GML, regional medical teams, and other internal stakeholders.
Lead end-to-end publication planning and execution across abstracts, posters, oral presentations, manuscripts, reviews, and other scientific communications, ensuring quality, consistency, timeliness, and compliance with applicable standards and policies.
Translate evidence gaps, clinical and real-world data, scientific literature, treatment guidelines, medical insights, and the competitive landscape into clear publication priorities and an integrated scientific narrative.
Partner with Global Medical, Development, Biostatistics, HEOR, RWE, and regional teams to align evidence-generation and publication plans, incorporate regional perspectives, and maximize the scientific value and impact of available data.
Provide scientific interpretation of clinical trial data, registries, real-world evidence, published literature, and other relevant data to guide scientifically rigorous, medically accurate, and balanced publications and scientific communications.
Lead cross-functional publication teams and governance processes, including author and agency management, publication timelines, review and approval workflows, congress planning, budget oversight, and risk identification and mitigation.
Engage external experts, investigators, treatment centers, professional societies, and other scientific stakeholders to inform publication strategy and support the development and execution of high-quality scientific publications.
Monitor emerging science, treatment paradigms, medical insights, society guidelines, and the external landscape, and incorporate relevant developments into the publications strategy.
Represent Vertex at scientific and medical forums, including congresses, scientific societies, and medical education forums, as appropriate.
Partner on the development of aligned medical content and scientific materials, including slide decks, FAQs, congress materials, and other external-facing resources, as needed.
Champion scientific integrity, transparency, ethics, compliance, patient focus, and Vertex values across all publication activities.