Publication Lead, Rare Genetic Diseases
Company: Takeda Pharmaceutical
Location: Bronx
Posted on: May 11, 2022
Job Description:
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's and . I further attest that all information I submit
in my employment application is true to the best of my
knowledge.Job DescriptionAbout the role:At Takeda, we are a
forward-looking, world-class R&D organization that unlocks
innovation and delivers transformative therapies to patients. By
focusing R&D efforts on four therapeutic areas and other
targeted investments, we push the boundaries of what is possible in
order to bring life-changing therapies to patients worldwide.Join
Takeda as a The Publications Lead (Rare Genetic Diseases) where you
will define and drive publication planning and delivery based on
medical strategies, publication obligations, and data generation
and availability. You will also act as a key partner to the Global
Medical Strategy Team. As part of the Publications, you will report
to Head, Global Publications and work with Publications & Global
Medical Strategy Teams.How you will contribute:
- The Publications Lead (Rare Genetic Diseases) understands how
publication activities contribute to the overall medical affairs
scientific communication plan for the assigned programs and
therapeutic area; develops and implements a strategic, compliant
and fit-for-purpose publication plan for the specified program and
collaborates with all levels of Medical Affairs (i.e., global,
regional, local), Clinical, Global Evidence Outcomes, medical
publications agencies and external authors to ensure of execution
the global publication plan.
- Ensure Takeda's company-sponsored publication activities are
conducted according to Good Publication Practices (including, but
not limited to ICMJE, GPP3, CONSORT, etc) and Takeda's Global
Publication Standard, SOP, and applicable practice guidelines.
- The assigned publication programs will be global, may be large
and complex, and of business importance to Takeda and Takeda's
reputation, requiring multi-functional leadership experience and
skills to achieve program goals
- Develop and manage product/disease area Global Publication
Strategies and Plans in coordination with relevant Global Medical
Teams. Work with GMA lead, and Regional Lead to align publication
plans across geographies. Identify, select, and manage 3rd-party
providers and independent contractors to ensure the timely delivery
of quality publications.
- Collaborate with external authors and journals in planning and
execution of scientific publication activities.
- Closely coordinate budget reporting; responsible for
appropriate tracking and reporting of transfer of value according
to applicable transparency rules and regulations (e.g., US Sunshine
Act).
- Act as first point of contact for affiliate offices, internal
business partners, and management on publication-related issues,
including, but not limited to, vendor access, training, system
issues, and good publication practices.
- Ensure and communicate regular updates to relevant key
stakeholders to facilitate ongoing functional and regional
planning.
- Track Global Publications metrics and provide reports to the
Group Lead and Head of Publications as required.
- Demonstrated ability to work across functions, regions and
cultures
- Functional level leadership with the ability to inspire,
motivate and drive results
- Excellent communicator, able to persuasively convey both ideas
and data, verbally and in writing
- Proven skills as an effective team player who can engender
credibility and confidence within and outside the company
- Ability to distill complex issues and ideas down to simple
comprehensible terms
- Demonstrates leadership presence and confidence
- Embraces and demonstrates a diversity and inclusion mindset and
role models these behaviors for the organization
- Builds teams across functions and geographies with individuals
who have the right skills and experience to deliver on key
organizational initiatives.Minimum Requirements/Qualifications:
- A relevant healthcare degree (M.D., Pharm.D., Ph.D., MS or RN)
is preferred. Knowledge of scientific publication planning
approaches is required
- 7 years (for Associate Director) publication experience in
medical communication agencies or biopharmaceutical industry,
preferably within a matrix structure.
- At least 3 years of experience in a medical affairs role (e.g.
Medical Information, Medical Communications, Medical Education,
Publications, Evidence Generation)
- Experience and knowledge of clinical trial reports, data
presentation, and interpretation
- Familiarity with regulatory and legal guidelines regarding
publication planning strategy and execution
- Experience leading cross-functional and global teams
- Experience managing vendors and complex projects
- Experience in Rare Genetic Diseases preferred, but not
required
- CMPP qualification preferredWhat Takeda can offer you:
- Comprehensive Healthcare: Medical, Dental, and Vision
- Financial Planning & Stability: 401(k) with company match and
Annual Retirement Contribution Plan
- Health & Wellness programs including onsite flu shots and
health screenings
- Generous time off for vacation and the option to purchase
additional vacation days
- Community Outreach Programs and company match of charitable
contributions
- Family Planning Support
- Flexible Work Paths
- Tuition reimbursementMore 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.Absent an approved
religious or medical reason, all US office-based and lab-based
Takeda employees who work fully on-site or in a hybrid model (as
determined by Takeda) must be fully vaccinated to work at a Takeda
site or to engage with Takeda colleagues or anyone else on behalf
of Takeda. US field-based employees must be fully vaccinated as a
condition of employment, absent an approved religious or medical
reason. US employees who work at a Takeda manufacturing facility,
and those who work at a BioLife center or BioLife lab, may be
subject to different guidelines. If you are contacted by a Takeda
recruiter about your job application, we encourage you to seek more
information on the applicable guidelines for the Business
Unit/Function to which you have applied.In accordance with the CO
Equal Pay Act, Colorado Applicants Are Not Permitted to
Apply.#LI-RMEEO StatementTakeda 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.LocationsCambridge, MAWorker
TypeEmployeeWorker Sub-TypeRegularTime TypeFull time
Keywords: Takeda Pharmaceutical, New Rochelle , Publication Lead, Rare Genetic Diseases, Advertising , Bronx, New York
Didn't find what you're looking for? Search again!
Loading more jobs...