Global Medical Communication & Publications Lead, Immunology

Takeda Pharmaceutical Co.; Kendall Square (MA); Sur place; USD 169 000 - 266 000; Plein temps

Résumé du poste

Takeda is seeking an Associate Director, Global Medical Communications & Publication Lead to develop and execute an integrated scientific communications plan for assigned assets, aligning with the medical strategy and evidence-generation plans. You will ensure data are translated into accurate, compliant communications across formats and channels.

You will lead publications, congress materials and medical education deliverables within a single plan, apply AI-enabled tools to improve efficiency,

Qualifications

• Bachelor's degree in life science or healthcare is required; advanced degree preferred (e.g., MSc, PharmD, PhD or MD).
• 3–5+ years in medical communications and/or publications within a global matrix environment; experience across both preferred.
• Knowledge of drug development, clinical data interpretation, evidence generation and medical strategy.
• Solid knowledge of medical review and regulatory/legal guidance for medical communications and of good publication practice and reporting guidelines (ICMJE); CMPP certification a plus.
• Demonstrated ability to lead cross-functional teams and influence without authority.
• Experience applying AI-enabled tools and digital technologies in scientific communications.

Responsabilités

• Develop and execute the integrated scientific communications plan for assigned asset(s).
• Lead development and maintenance of SCPs, lexicons, core slide decks and FAQs; deliver the global publication plan (abstracts, manuscripts, congress presentations, plain language summaries).
• Plan and execute congress and medical education activities for assigned asset(s).
• Lead cross-functional planning with Medical Affairs, Clinical Development, Biostatistics, evidence generation, regional/local teams and external authors.
• Provide medical review of promotional and non-promotional materials with Legal and Regulatory to ensure compliant communication.
• Ensure publications adhere to SOPs, GPP, ICMJE and reporting guidelines, with appropriate authorship and disclosure.
• Prepare briefs and source packages for GCC and Medical Content Factory; identify reuse opportunities.
• Pilot and apply AI-enabled tools and digital channels to improve planning, content development, visualization and review.
• Track KPIs and integrate insights into plan updates.
• Manage budget, forecasts, timelines and vendors for assigned asset(s).
• Provide matrix leadership, coaching or mentoring to managers, fellows and contributors.

Formation

Bachelor's degree in life science or healthcare

Advanced degree (e.g., MSc, PharmD, PhD or MD)

Description du poste

About the Role:

The Associate Director, Global Medical Communication & Publication Lead develops and executes the integrated scientific communications plan, spanning medical communications and publications, for assigned asset(s) or program(s), in alignment with the asset medical strategy and with Group Lead guidance on broader TA decisions.

Ensures evidence for assigned asset(s) is translated into accurate, compliant and audience-relevant communications and publications, delivered in the right format, through the right channels, at the right time.

Leads core scientific content, publications, congress and medical education deliverables as one integrated plan.

Applies AI-enabled tools and digital channels within assigned scope to improve efficiency, quality and stakeholder engagement.

How You Will Contribute:

Develop and execute the integrated scientific communications plan for assigned asset(s), aligned with medical strategy and evidence-generation plans and supporting a consistent omnichannel HCP experience across publications, core content and digital channels; drive prioritization, timelines and decisions within scope.

Lead development and maintenance of SCPs, lexicons, core slide decks and FAQs, and deliver the global publication plan (abstracts, manuscripts, congress presentations, plain language summaries), ensuring one consistent scientific narrative.

Plan and execute congress and medical education activities for assigned asset(s), including booth content, symposia, FAQs and insight collection.

Lead cross-functional planning with Medical Affairs, Clinical Development, Biostatistics, evidence generation, regional/local teams and external authors; influence without authority to align priorities and timelines.

Provide medical review of promotional and non-promotional materials, partnering with Legal and Regulatory to ensure accurate, balanced and compliant communication.

Ensure publications adhere to SOPs, GPP, ICMJE and reporting guidelines, with appropriate authorship and timely disclosure.

Prepare clear briefs and approved source packages for the GCC and Medical Content Factory; identify reuse opportunities and plan derivative needs up front.

Pilot and apply AI-enabled tools and digital channels to improve planning, content development, visualization and review within assigned scope.

Track agreed KPIs and integrate field, congress and digital insights into plan updates.

Manage budget, forecasts, timelines and vendors for assigned asset(s); identify risks and elevate appropriately.

Provide matrix leadership, coaching or mentoring to managers, fellows and contributors as appropriate.

Preferred Qualifications:

Bachelor's degree in a life science or healthcare discipline required; advanced degree preferred (e.g., MSc, PharmD, PhD or MD).

Minimum relevant experience: Bachelor's degree + 10 years, Master's degree + 8 years, or Doctorate + 6 years in the biopharmaceutical industry or a closely related field.

3-5+ years in medical communications and/or publications within a global matrix environment; experience across both preferred.

Strong knowledge of drug development, clinical data interpretation, evidence generation and medical strategy.

Solid knowledge of medical review and regulatory/legal guidance for medical communications, and of good publication practice and reporting guidelines (e.g., GPP, ICMJE); CMPP certification a plus.

Demonstrated ability to lead cross-functional teams and influence without authority.

Makes decisions within assigned scope, identifies risks, proposes solutions and escalates appropriately; experience coaching or mentoring others.

Experience applying AI-enabled tools and digital technologies in scientific communications.

Excellent written, verbal and presentation skills; translates complex data into clear communications.

Experience in the assigned therapeutic area a plus.

Domestic and international travel required (up to ~20%), including congresses and offsite meetings.

Takeda Compensation and Benefits Summary

• For Location: USA - MA - Cambridge
• U.S. Base Salary Range: $169,400.00 - $266,200.00
• The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
• The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

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 USA - MA - Cambridge

Worker Type Employee

Worker Sub-Type Regular Time Type Full time Job Exempt Yes

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.

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.

Takeda is an equal opportunity employer.