14 days old

Manager, GMA Evidence Generation Operations

Takeda Development Center Americas, Inc.
Boston, MA 02109
  • Job Code
    R0038450

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Job Description

Manager, GMA Evidence Generation Operations

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Manager, GMA Evidence Generation Operations in our Boston, MA office.

At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Here, you will be a vital contributor to our inspiring, bold mission.

As a Manager, GMA Evidence Generation Operations working on the Global Medical Evidence team, you will be empowered to manage all aspects of assigned program including Medical Affairs Company Sponsored Studies (MACS), Investigator Initiated Research (IIR), and Externally Sponsored Collaborative Clinical Research (CCR) studies for assigned therapeutic areas and product programs. A typical day will include:

POSITION OBJECTIVES:

  • Manage all aspects of FMV for MACS, Collaborative Research and IIR.
  • Manage TA and product level study budgets and communicate study activities to internal stakeholders.
  • Oversee and manage the activities of Operations project managers, including the initiation, tracking, completion, and reporting of studies.
  • Responsible for the conduct of studies in accordance with all applicable internal legal and compliance policies (SOPs) as well as external regional and country specific regulatory guidelines.
  • May serve as the therapeutic operational area lead for interfacing with internal stakeholders (e.g. GMA, Region and LOC medical leads, TA Medical Heads, alliance partners, etc.) and external investigators to develop and execute research plans and budgets.

POSITION ACCOUNTABILITIES:

  • Lead receipt, processing, and internal cross-functional review of internal/external study submissions
  • Oversee the conduct of FMV assessments of budgets submitted for approved studies in accordance with Takeda policies and procedures.
  • Review and approve research committee materials including study concepts and protocols, meeting minutes, and investigator communications.
  • Lead required cross-functional review meetings to review, approve, and track studies and ensure proper documentation and archiving (minutes, team communications, etc.) of review outcomes.
  • Coordinate the capture, archiving and reporting of appropriate study level information (including patient safety information).
  • Oversee and/or facilitate the management of the internal ienvision (or equivalent system) and document repositories per Medical Affairs SOPs and processes.
  • Coordinate with Pharmacovigilance and Regulatory Affairs to respond to external audits and requests from external regulatory bodies.
  • Contribute to pre- fair market value (FMV) evaluation of proposed study budget and oversee the conduct of FMV assessments of budgets submitted for approved studies in accordance with Takeda policies and procedures.
  • Manages all finance related aspects for global studies invoicing, accruals and forecasting

EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:

  • Minimum MSc degree required (preferably PhD), preferably in a health sciences related field with 3 years of research related experience and/or pharmaceutical industry experience.
  • Proven track record of strong leadership, project management and demonstrated ability to coach and mentor individuals.
  • Ability to communicate and interact thoughtfully, transparently, and appropriately with a variety of clients both internal and external to Takeda.
  • Experience overseeing work of and mentoring other individuals with a variety of scientific and non-scientific backgrounds and training
  • Research experience (health sciences related), Pharmaceutical Industry including CRO
  • Experience working in a global organization highly desirable.

This job posting exclude Colorado applicants.

TRAVEL REQUIREMENTS:

  • Ability to drive or fly to various internal and external meetings.
  • Required travel approximately (0 - 10%), including international trips, overnight stays, and some weekend commitments.

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 Programs

Empowering Our People to Shine

Discover more at takedajobs.com

No Phone Calls or Recruiters Please.

*RM-LI

Locations

Boston, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time





Posted: 2021-06-07 Expires: 2021-07-06
Sponsored by:
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Sponsored by:
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Manager, GMA Evidence Generation Operations

Takeda Development Center Americas, Inc.
Boston, MA 02109

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