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Scientific Communications Group Lead, GI Oncology (Director)

Takeda
8 hours ago
Remote friendly (Cambridge, MA)
United States
$192,400 - $302,390 USD yearly
Medical Affairs
Responsibilities
- Provide leadership as Scientific Communications Group Lead for Gastroenterology (GI) within Global Medical Affairs.
- Own and execute scientific communications strategies and deliverables, including all GI Franchise publication activities (marketed and pipeline).
- Manage team/talent, resources, vendor capabilities, and compliance-ready systems/policies/SOPs to ensure timely and compliant delivery.
- Oversee development and execution of global scientific communication plans (e.g., publications, slide decks, field medical resources, training materials, congress activities, satellite symposia, website content).
- Partner cross-functionally with medical affairs, clinical development, outcomes research, commercial, and corporate communications.
- Align GI scientific communications plans with product medical strategies and disease area strategies.
- Lead/ensure quality and consistency of strategic scientific communications and publications at all organizational levels; lead change management as needed.
- Manage financials (budgets, work orders, vendor performance management) and ensure projects stay within strategy and budget.
- Provide medical/scientific review of materials as needed and ensure adherence to relevant laws, regulations, and publication ethics.
- Conduct internal training on publication processes and guidelines; serve as liaison with external content contributors.

Qualifications (Minimum Requirements)
- Advanced degree (PhD, PharmD, MD, or equivalent) preferred; otherwise Masterโ€™s degree plus commensurate long-term pharma/biotech experience.
- 7+ years healthcare/related experience; 5+ years in developing and executing scientific communications deliverables (including publications) in medical affairs/pharma/biotech or a medical communications agency (essential).
- 3+ years budgetary and/or people management experience.
- Knowledge of scientific publication planning approaches and ability to apply external guidelines.
- Knowledge of good publication practice (GPP22), ICMJE, and CONSORT.
- Solid publication management experience and knowledge of scientific platform software/systems.
- Vendor management experience.
- Strong communication, prioritization, problem-solving, planning, and organizational skills.
- Understanding of drug development, clinical trial design, product lifecycle, statistics, and trial data reporting.
- Strong analytical skills for interpreting/presenting complex data.
- Experience managing budgets to performance targets.
- Advanced PC skills: MS Word, Excel, PowerPoint, SharePoint.

Preferred
- Oncology experience.

Skills/Competencies
- Strategic approach, collaboration in matrix environments, inspires teams, drives results with metrics, creativity/innovation (data analytics/publication planning).
- Compliance and regulatory understanding.

Travel
- Up to 20% domestic and international travel.

Application Instructions
- Apply via the โ€œApplyโ€ button; by doing so you acknowledge and consent to the application process and processing of your information per Takedaโ€™s Privacy Notice and Terms of Use, and attest the information you provide is true to the best of your knowledge.