Associate Director, Scientific Communications Lead, Lung, Global Medical Affairs Oncology

Location:

Boston, Massachusetts, United States Salary: $ - $Company:
Takeda Pharmaceutical Co.Posted:

Job Description As part of the Global Medical Affairs Oncology team, you will report to the Scientific Communications Group Lead, Lung and help advance Takeda Oncology’s vision to cure cancer. As a subject matter expert in publication best practices and scientific communications strategy, you will proactively define, own, and drive the integrated publication and scientific communication strategy, plans, and deliverables for assigned oncology assets, aligned with medical strategy, transparency requirements, data availability, and business priorities.

You will be accountable for timely, accurate, scientifically rigorous, and compliant execution and for maintaining a consistent scientific voice across channels.

You will lead cross-functional publication planning and partner with Global Medical Affairs, Clinical Development, Outcomes Research, regional and local teams, authors, investigators, opinion leaders, and affiliates. You will oversee the end-to-end development of publications for external audiences and a broad range of medical communications deliverables, including scientific platforms and narratives, congress materials, slide decks, pathway and guideline submissions, training resources, animations, and digital amplification of data.

You will also manage agency partners, publication systems, budgets, timelines, risks, and quality standards, serving as the primary point of accountability for assigned programs.

How You Will Contribute Develop and execute publication and scientific communication plans in partnership with cross-functional teams to support product medical strategies.

Lead publication planning activities by coordinating content development, timelines, and stakeholder alignment across assigned programs.

Review scientific publications and materials to ensure accuracy, scientific rigor, and compliance with applicable standards and requirements.

Partner with authors and external experts to facilitate content development and support effective scientific communication.

Oversee vendors and publication resources to support delivery of publication plans, budgets, and operational objectives.

Develop scientific communication materials including presentations, training resources, and other medical affairs content.

Provide guidance and training to colleagues on publication strategy, execution best practices, and good publication practices.

Qualifications Advanced degree (PhD, PharmD, or equivalent) in a scientific discipline (preferred) or a minimum of Bachelor’s degree in a scientific discipline plus commensurate long-term experience within pharmaceutical or biotech industry

At least 5 years of healthcare or related experience, including 3 years of experience developing and executing medical publications within the pharmaceutical or, biotechnology industry, or within a medical communications agency, is essential.

Knowledge of the scientific publication planning processes, current standards of good publication practice (GPP3), pertinent external guidelines related to industry publications (ICMJE), and scientific reporting standards for studies (CONSORT)
Oncology experience strongly preferred

Experience managing multiple projects and delivering high-quality work in a fast-paced environment.

Strong written and verbal communication skills with the ability to interpret and communicate complex scientific and medical information.

Experience managing external vendors, resources, or service providers to support program objectives.

Understanding of pharmaceutical clinical development, clinical trial design, statistical methods, and clinical data reporting requirements.

Experience in medical communications…