Associate Director, Scientific Communications Lead, Hematology, Global Medical Affairs Oncology As a member of Takeda Oncology, your work will contribute to our bold, inspiring vision: We aspire to cure cancer. You will build a career grounded in purpose and be empowered to deliver your best. Your role defines and drives the publication and scientific communication strategic plan and deliverables for the oncology assets based on medical strategies, transparency requirements, and data availability.

How You Will Contribute

Collaborate with cross-functional, multidisciplinary teams to support the development, management, and execution of global strategic scientific communication & publication plans that align with product medical strategies.

Proactively develop, manage, and execute on global or regionally integrated strategic publication plans and scientific communication plans in coordination with cross-functional teams, ensuring alignment with product medical strategies.

Have a strong understanding of prioritized disease areas, including landscape and competition.

Initiate communication with authors; identify all necessary data required for content development; participate in author meetings to facilitate content discussion and ensure appropriate content development process is followed.

Critically review publications including manuscripts, abstracts, posters, and oral presentations for accuracy and scientific rigor; manage and facilitate the content review process, including collating reviewer comments and having discussions with authors and reviewers.

Commitment to ethical practices in the preparation and dissemination of publications.

Effectively and consistently communicate the publication and scientific communications strategy, tactical plan, and plan progress to internal business partners; work with vendors and internal technical support groups to evaluate and optimize publications systems for reporting metrics to meet stakeholder needs.

Manage medical writing agency, including oversight on execution of publications plans and budget, and maintenance of publications management databases such as Datavision.

Ensure compliance with all applicable laws, regulations, and policies for development, internal review, and dissemination of scientific communications materials, and act with commitment to ethical practices in the preparation and dissemination of publications.

Manage alliance partnerships.

Evaluate trends in medical publications and drive opportunities for enhanced publications content and amplification of publications to increase value of publications in scientific exchange; lead and participate in process development and refinement, as needed.

Lead or participate in recruitment of vendors to fill resource gaps.

Provide guidance and training to colleagues on publication strategy development and tactical execution best practices.

Coordinate, plan, and manage scientific communications budget for assigned program(s) in close collaboration with GMAO Operations team.

As needed, provide medical and scientific review of Global Medical Affairs Oncology materials (and, if required, promotional materials) to support the medical (and promotional) review process.

As a subject matter expert for the assigned programs, lead or contribute to the development of content for Global Medical Affairs projects, including but not limited to NCCN compendia, training materials, global congress plan, and medical resource tools, as needed.

Serve as the Global Scientific Communications representative on relevant Global Medical Strategy Team.

Attend conferences, symposia, or other meetings, as necessary or as assigned, and act as liaison between Global Scientific Communications and external content contributors.

Basic 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.

5+ years healthcare or related experience, including 3+ years of experience with the development and execution of medical publications within medical affairs in the pharmaceutical or biotech 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.

Strong written and verbal communication skills with demonstrated ability to manage several projects simultaneously.

Ability to work well independently and under pressure.

Strong capabilities and experience with resource allocation and vendor management.

Ability to synthesize, interpret, present, and discuss complex medical and scientific data.

Understanding of pharmaceutical clinical development and product life‑cycle management, clinical trial design and execution, statistical methods and clinical trial data reporting requirements.

Experience in medical communications function, which may include publications, medical information, and/or training.

Experience with publications management databases such as Datavision.

Working experience in cross‑functional teams and global/local teams within the pharmaceutical or related industry.

Competencies

Strategic Approach: Ability to identify opportunities and anticipate changes in the business landscape through an understanding and ongoing assessment of the environment.

Collaboration: Ability to cultivate a broad network of relationships throughout the organization, connecting global, regional and local organizations. Requires experience and success in working in a matrix, cross‑functional environment; excellent collaboration skills; experience working across functions to achieve results.

Engage Others: Ability to create a clear and unifying vision inspiring teams to excel.

Drive for Results: Creates functional strategies and goals that are closely aligned with company objectives and develops metrics to track and assess performance.

Creativity and Innovation: Ability to contribute to data analytics and publication planning, including ideas for sub‑analyses.

Compliance and Regulatory: Excellent understanding of regulatory, compliance and legal requirements.

Technical Skills: Advanced PC skills, including Datavision, MS Project, Word, Excel, Power Point, and SharePoint.

Travel Requirements

Up to 10% domestic and international travel required.

More About Us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient‑focused company that will inspire and empower you to grow through life‑changing work. This position is currently classified as “hybrid” in accordance with Takeda’s Hybrid and Remote Work policy. Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Compensation Location: Boston, MA

U.S. Base Salary Range: $168,700.00 – $265,100.00.

U.S. based employees may be eligible for short‑term and/or long‑term incentives, health benefits, 401(k) match, short‑term and long‑term disability, life insurance, tuition reimbursement, paid volunteer time, holidays, and well‑being benefits. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires accrue up to 120 hours of paid vacation.

EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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