By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Noticeand Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Join Takeda as an Associate Director, US Medical Communications, Rare Diseases and PDT out of our Lexington, MA office. Where you will be a strategic partner of the US Medical Communications team responsible for supporting the development and execution of the medical communications strategy across the Rare Diseases and Plasma Derived Therapies (PDT) portfolio. You will also You will also actively be involved in the medical communications Scientific Communication Platform (SCP) and Integrated Communication Platform (ICP) development, and content generation, which may include, but is not limited to, publications, scientific slide decks, field medical tools, training materials, congress-related activities, websites/tools, and other medical programs. You will also support the execution of key medical communications tactics and activities, in an independent manner, closely coordinated with the Director US Medical Communications and Scientific Training. will interact with key internal stakeholders, which may include members of the US Medical Communications Team and other functional medical partners such as Medical and Scientific Directors, Outcomes Research, Field Medical, Medical Information, Program Management; other USBU Stakeholders; and Global functional groups such as Medical, Publications, Regulatory, Statistics, and Legal.

How you will contribute:

• Involved in planning, development, and implementation of medical communication plans and education programs for assigned brands and/or pipeline therapies
• Maintain in-depth knowledge of medical communications trends and materials (scientific platform, core slide decks, scientific communication plans, digital communication plans) and can independently drive updates/revisions to these materials
• Maintain the scientific accuracy and robustness of the information included in the SCP and Core Communication Objectives (CCOs) for assigned products, and in close collaboration with the cross-functional team supports the development of new SCPs for new products
• In collaboration with the US Medical Affairs team, support development and execution of the Medical Communications plan and associated activities, such as generation of core Medical Communication documents, SCP, ICP, medical booths and other congress activities, satellite symposia, educational activities, and scientific meetings with external experts
• Support congress planning and execution including oversight of content and design for the medical affairs booth, collection and generation of scientific insights, and planning of scientific symposia
• Drive post-congress support including liaising with competitive intelligence and post-congress integration of learnings into medical materials and communication plans
• Support medical review during the promotional and non-promotional (e.g., disease state) commercial material review, as well as medical affairs material review, for assigned brands
• Assist in scientific or medical content development for training materials for assigned therapeutic area
• Ensure that assigned medical communication projects remain on strategy, within budget, and are executed in a timely manner

Minimum Requirements/Qualifications:

Required:

• Advanced degree (i.e., MPH, MS, Ph.D., MD, or PharmD) in a biosciences discipline
• 4+ years of related experience at a pharmaceutical company or a medical communications agency
• 3+ years in medical affairs including roles in medical communication function
• Experience leading individuals and cross-functional teams
• Successful track record of implementing medical communication and congress programs, including omnichannel communication and digital channels/tools
• Excellent written and oral communication skills
• Ability to work across diverse therapeutic areas
• Experience with resource allocation and vendor management
• Experience with managing budgets
• Travel- Ability to travel to various professional meetings and conferences – limited overnight. Some international travel may be required.

Preferred:

• Understanding pharmaceutical clinical development and product life-cycle management
• Strong self-motivation and enthusiasm with demonstrated ability to thrive in a fast-paced, dynamic, highly detail-oriented environment
• Ability to understand and interpret medical/scientific data and develop strategic messaging and strong knowledge of pharmaceutical standards, compliance, and regulations
• Strong experience in writing scientific communication decks, reports, materials for educational activities

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.

Certified as a Global Top Employer, 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.

This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

U.S. Base Salary Range:

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.

Locations

Worker Type

Worker Sub-Type

Time Type