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Senior Manager, PV Operations

Remote
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  • Job Level: Senior
  • Travel: Minimal (if any)

Takeda has been translating science into breakthrough medicines for 240 years. Every step of the way, our teams have worked together to tackle some of the most challenging problems in drug discovery and development. Today, we’re a driving force behind innovative therapies that make a lasting difference to millions of patients around the world.

In R&D, all of our history and potential comes together in an environment that welcomes diversity of thought and amplifies every voice. Working closely with colleagues, you’ll play a key role in bringing our rich pipeline of products forward to help patients. Come join a team that’s earned trust for more than two centuries, and find out how advancing transformative therapies at Takeda will shape your bright future.

Job ID R0140045 Date posted 12/10/2024 Location Remote

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

OBJECTIVE:

  • Serve as a primary liaison and point of contact for vendor operations and vendor oversight, including vendors performing case management, case intake (i.e., Call Centers), scientific literature review, etc.

  • Oversee operations performed by the PV BPO vendor including contract compliance, quality and timeliness of deliverables

  • Serve as the primary liaison and point of contact for vendor operations including the PV BPO vendor and/or vendors performing case management, case intake, literature review; call centers

  • Provide Subject Matter expertise (SME) during audits and inspections in the areas of case processing/case management activities, literature monitoring, legal case processing, vendor oversight, etc.

ACCOUNTABILITIES:

  • Provide leadership and oversight on case management for the Global PV Operations Team to ensure adverse event information is processed according to company timelines and quality standards

  • Oversee regulatory submissions for ICSRs from the Global Safety database, on-time delivery of adverse event reports to global Health Authorities, alliance partners, local operating companies (LOCs) including SUSAR and SAE communication to ECs and investigators as applicable

  • In partnership with the Global Standards and Compliance team, direct and manage communication with alliance partners, LOCs and CROs regarding the evaluation and processing of ICSRs

  • In partnership with the Global Standards and Compliance team, lead and direct the review and approval of alliance partner safety data exchange agreements for the inclusion of appropriate safety reporting requirements

  • Ensureoverall performanceofthedepartmentand compliance with global regulatory requirements by implementation of appropriate SOPs, processes, metrics, and monitoring of performance and compliance, and training at a global level

  • Oversee and direct reconciliation processes for case exchange with LOCs and alliance partners

  • LeadPV relationshipwithPVBPOvendorand/orvendorsperformingcase management to ensure compliance with SLAs

  • Support LOCs in PV tasks respondingto queriesand requests regarding case handling

  • Interfacewithcommercialqualityforproductcomplaints;assistinobtainingfollow-upwhennecessaryforadverseevents,productqualitycomplaintsor other safely information

  • Directrelationshipwith and outputofBPOpartner(s)in accordancewith SLA

  • Liaiseswithfinancial/projectmanagementforbudgetplanning

  • Approveactualinvoicesandconfirmaccuracyofspendandbills

  • Coordinate clinical and project management case processing teamstoassess/predictcasevolumestoensurestaffingplanning at vendor

  • Leadplanningforad-hoccaseprocessingrelatedprojects e.g.

  • Legal cases or AE/SAEs generated through marketing surveys

  • Lead and facilitate regular joint operating committee meetings to review / address issues if needed for: Adherence to KPIs and SLAs. Forecast demand. Issueescalations.Continuousimprovement initiatives. Change management

  • Manage/reviewdeliveryagainstMSAterms

  • Monitor global KPIs and SLAs

  • Ensure quality of deliverables across teams

  • Represent voice of vendor to PV function

  • Provide guidance to delivery teams

  • Maintain operating manual (describing operating rules with vendor)

  • Lead change management and ongoing training

  • Establish and manage vendor oversight procedures

  • Partner with QA to establish and manageBPO vendorqualityagreement procedures include vendors performing case management/intake activities or literature review and surveillance

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

  • Bachelor’s required. Advanced degree in scientific/medical field preferred

  • Minimum6yearspharmaceuticalorhealthcarerelatedindustryexperience required

  • Minimum 5 years PV experience with 3 years experience working with CROs, vendors, and relationship management required

  • GlobalexperiencewithCROs,vendorsandrelationshipmanagement preferred

  • Good cross cultural understanding and experience

  • Experience in people management and well developed skills in teambuilding, motivating and developing people

  • Demonstrated skills in negotiation and consensus decision making

  • Criticalthinkingandanalyticalskillsandabilitytomakekeydecisions

  • Demonstrated effectiveness in external partner relationship management

  • Understandingofmedical/scientificterminology

  • GoodknowledgeofPVregulationsfortheglobalpre-andpost-market, i.e. FDA, EMA, ICH GVP

  • Experience with safety databases, including MedDRA and WHO Drug

  • Excellent written/oral communication skills

  • Accuracyandattentiontodetail

  • Flexible mindset

  • Team worker with collaborative approach

  • Ability to prioritize under pressure

  • Welldevelopedorganizational skills


LICENSES/CERTIFICATIONS:

  • RN or Pharmacist preferred

TRAVEL REQUIREMENTS:

  • Some travel to global Takeda sites may be required

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:

Massachusetts - Virtual

U.S. Base Salary Range:

133,000.00 - 209,000.00

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.

U.S. based employees may be eligible for short-term and/or long-termincentives. U.S.based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S.based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

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

Massachusetts - Virtual

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

Yes

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During my 20-year journey here, I’ve been fully supported by my colleagues, and I can’t say enough about our rich internal talent and the long-standing values that drive our decisions as we work to develop important medicines for the patients we serve.

Doug Coffman - Head, R&D Asset Transition & Integration Office, R&D Regional & Business Operations

When making any type of decision, the first thing we ask is 'how will this impact patients?’ Ultimately, we’re laser focused on the best interests of the patient, and I truly believe we follow through on that.

Meredith Culp - VP, Head of Neuroscience Therapeutic Area Strategy & Operations and Head of Global Development Integration Office

Our culture and shared values make us like a family here at Takeda. It doesn't feel like work when you're doing something you love with people you love, and when your outcome is really fantastic.

Alison Handley, Head, Center for External Innovation

The heart of our work

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What we believe in

Our values of Takeda-ism are Integrity, Fairness, Honesty and Perseverance, with Integrity as the core. These are brought to life through actions based on Patient, Trust, Reputation and Business, in that order.

Our belief in putting people first extends beyond our patients — it includes their families and communities, as well as our Takeda colleagues and their families.

We are committed to embracing our differences, valuing different perspectives, and fostering a culture of respect, inclusiveness and empowerment.

Our embedded Diversity, Equity & Inclusion (DE&I) strategy enables us to attract and retain exceptional talent, drives innovation, and helps address systemic inequalities in our communities.

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Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.

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