Associate Director, Pharmacovigilance Business Partner Relations
Company: Takeda Pharmaceutical
Location: Jersey City
Posted on: May 10, 2022
Job Description:
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with Takeda's Privacy Notice and Terms of Use. I further attest
that all information I submit in my employment application is true
to the best of my knowledge.Job DescriptionAre you looking for a
patient-focused company that will inspire you and support your
career? If so, be empowered to take charge of your future at
Takeda. Join us as an Associate Director, Pharmacovigilance
Business Partner Relations in our Cambridge, MA office.Associate
Director of PV Business Partner Relations oversees global strategic
initiatives and operational aspects of alliance management. Primary
responsibilities include but are not limited to:
- Lead at a high-level, PV alliances/partnerships and associated
business activities, including agreements
- Proactively develop and implement process improvement and
increased efficiencies for global PV
- Lead and/or significantly contribute to PV due
diligence/business development activities
ACCOUNTABILITIES:
- Develop and implement a scalable process for managing and
tracking safety exchange agreements/documents (PVAs / Safety Data
Exchange Agreements / SDEA)
- Review and provide input on PVAs and associated Agreements
- Collaborate with the PV Compliance group to address and resolve
compliance issues associated with PVAs
- Partner with key stakeholders to contribute to the development
and maintenance of a global PVA template
- Support the local Drug Safety Officers DSOs in Agreement
activities as needed
- Oversee the overall operational aspects of global PV alliances
- Participate in meetings related to partner alliance and
cross-program global operations as required.
- Identify and work to resolve issues in PV
alliances/partnerships.
- Escalate issues in PV alliances to senior management as
appropriate.
- Oversee vendors handling PVA/alliance management activitiesDue
Diligence/Alliance Management
- Oversee the operational aspects of global PV alliances.
- Participate in joint company/alliance management meetings as
needed
- Work to resolve issues regarding PV alliances
- Lead and/or provide strategic contributions to PV due
diligence/business development activities
- Product/company acquisition or licensing
- Due diligence activities for global PV
- Due diligence process documentsGeneral
- Escalate issues/problems to senior management as needed
- Any other tasks assigned by manager to assist in departmental
activitiesEDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:
- Bachelor's required. Post-graduate degree or equivalent
(Masters Degree/MBA) preferred
- Experience in, but not limited to, developing PV safety
agreements, safety team charters, service level experience
- Experience in and knowledge of due diligence for company
acquisitions and/or licensing partnerships
- Product development including clinical safety experience
- Ability to interact effectively with staff of multiple
disciplines both within and outside the company both nationally and
internationally
- Demonstrated ability and experience leading high performing
teams internally and cross functionally in a global highly matrixed
and collaborative environment
- Ability to proactively identify and anticipate risks associated
with non-adherence to the regulations
- Strong understanding and knowledge of the business areas both
internally within the organization and touch points externally
- Excellent time management skills
- Self starter and strategic thinker
- Able to lead teleconferences and meetings
- Project management training and experience
- Proven ability to create and implement operational
efficiencies
- Excellent oral and written communication skills
- Strong relationship management skills
- Expertise in clinical research and product safety activities in
the pharmaceutical industry
- Ability to handle confidential information appropriately
- Preferred experience in vendor management
- Minimum 8 years of experience in pharmaceutical/biotech
industry or a minimum 3 years of experience in pharmacovigilance,
clinical research, or alliance management role with advanced
degreeTRAVEL REQUIREMENTS:
- Estimated up to 5 travel times per year, including possible
international travel.WHAT TAKEDA CAN OFFER YOU:
- 401(k) with company match and Annual Retirement Contribution
Plan
- Tuition reimbursement
- Company match of charitable contributions
- 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 ProgramsEmpowering Our People to ShineLearn
more at takedajobs.com.Takeda is an EEO employer of minorities,
women, disabled, protected veterans, and considers qualified
applicants with criminal histories in accordance with applicable
laws. For more information, visit
http://www.takeda.us/careers/EEO_Policy_Statement.aspxNo Phone
Calls or Recruiters Please.#LI-MT1EEO 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.LocationsMassachusetts -
VirtualWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull
time
Keywords: Takeda Pharmaceutical, Jersey City , Associate Director, Pharmacovigilance Business Partner Relations, Executive , Jersey City, New Jersey
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