Alliance Management Specialist, Pharmacovigilance
Company: Jazz Pharmaceuticals
Location: Philadelphia
Posted on: August 7, 2022
Job Description:
Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global
biopharmaceutical company whose purpose is to innovate to transform
the lives of patients and their families. We are dedicated to
developing life-changing medicines for people with serious diseases
- often with limited or no therapeutic options. We have a diverse
portfolio of marketed medicines and novel product candidates, from
early- to late-stage development, in neuroscience and oncology. We
actively explore new options for patients including novel
compounds, small molecules and biologics, and through cannabinoid
science and innovative delivery technologies. Jazz is headquartered
in Dublin, Ireland and has employees around the globe, serving
patients in nearly 75 countries. For more information, please visit
and on Twitter. The PV Alliance Management (PVAM) Specialist plays
a key role in the PVAM Team, facilitating across functional teams,
building relationships, and supporting the delivery of high quality
PV Agreements to ensure timely and accurate collection, safety
review, processing and reporting of adverse event data in
compliance with applicable global regulations and Jazz
Pharmaceuticals standard operating procedures and guidelines. To
this end, the PVAM Specialist guides and facilitates effective
working relationships within R&D Global Pharmacovigilance and
Labeling, and cross-functionally with strategic departments within
the company and its affiliates/subsidiaries to foster smooth,
accurate, and timely flow of activities related to PV Agreements
(PVA)s as well as effective contractual relationships with PV
Service Providers. The PVAM Specialist is versed on PVAs, Safety
Reporting Plans (SRPs), PV Service Provider Agreements, and acts as
key contact person for internal and external customers, managing
these alliances directly and working with the PVAM Team as well as
in partnership with cross-functional staff. Working with the PVAM
Manager, the Specialist may negotiate and maintain Agreements,
including maintenance and reporting of KPIs/SLAs and participate in
vendor governance. The Specialist will be responsible for
coordinating PV activities related to Global Expansion in Canada
and US. The PVAM Specialist may assist in special projects as
assigned by the Pharmacovigilance (PV) department management.The
PVAM Specialists have a breadth of responsibilities which are
prioritized within the PVAM Team, and may be assigned to:
- Business Development & Opportunities
- Global PV Vendor Services
- Regional PV Vendor ServicesPVAM Specialist responsibilities may
include PV alliance activities such as, but not limited to:
- Serve as the liaison between Global Pharmacovigilance and cross
functional organizations, acting as a Pharmacovigilance ambassador
and domain expert as well as increasing awareness within Global
Pharmacovigilance of cross-functional customer/stakeholder needs
and dependencies, including PV Service providers.
- Support implementation for new partnerships and
maintenance/change
- Support establishment and maintenance of PVAs/SRPs/SPOPs/WOs
associated with new business initiatives and opportunities.
- Interact with business process owners for additional
information to address questions in establishing a
PVA/SRP/SPOP/WO.
- Coordinate the PVA/SRP review by the safety review team,
summarize agreement comments, and participate in the negotiation of
the agreement.
- Contribute to resolving conflicts at team level or higher and
facilitate decision making within the team. Escalate issues
utilizing governance models and standard communication plans.
- Coordinate implementation of Safety Reporting plans for
programs with the potential to generate safety information.
- Coordinate PV activities associated with in/out-licensing and
marketing authorizations/withdrawals in Canada and United
States.
- Collaborate with the cross-functional groups that have
responsibility for activities that may generate adverse events or
safety information such as (not limited to) Business
Alliance/Development, Commercial, Medical Affairs.
- Support collection of information required to update designated
sections of the PSMF.
- Organize and moderate meetings and author minutes/discussion
summaries. Solicit items for and set agendas. Send out draft
minutes/summaries for comments to both internal Global
Pharmacovigilance and external PV Service Providers, and distribute
final summaries to all participants, as well as senior PVAM staff.
Follow up with meeting participants on the resolution of action
items from meetings.
- Maintain and organize internal PVAM files (Agreements,
supporting documents, meeting minutes).
- Participate in maintaining PVAM Jazz Portal and Mailbox.
- Conduct ad hoc/special projects and analyses for PVAM
management.PVAM Specialist Essential Functions
- Adheres to company templates and GxP guidelines for
documentation and communications
- Ensures compliance with corporate and departmental policies,
standard operating procedures, and timely completion of all
assigned training
- Other duties as required to support PVAM team
- Participate in the development and maintenance of PVAM activity
workflow processes, department policies, work instructions,
standard operating procedures and training material when new and/or
updated processes are introduced
- May serve as an individual contributor or a project manager for
functional projects or workflows.
- May mentor other team members
- Participation in Inspections and Audits as identified, as well
as active role in maintaining a business as usual inspection ready
state of operating
- Takes responsibility for personal development and continuous
improvement including keeping up to date with pharmacovigilance
practices, legislation and guidelines.
- Work collaboratively with cross-functional teams to evaluate
the performance, identify bottlenecks, minimize regulatory risks
and recognize patterns of inefficiencies in current operational
processes
- Collaborate effectively with Quality Assurance, Legal, and
Project Management. Minimum Requirements
- BS/BA degree in health related or biological science related
field
- 3 plus years of pharmaceutical drug safety/pharmacovigilance
operations experience
- In depth knowledge of pharmacovigilance activities and
processes, with a preference for experience in more than one PV
functional area
- Knowledge of current and emerging regulatory requirements and
expectations including EMA GVP Modules, FDA IND and NDA reporting
requirements, global risk management requirements, ICH, CIOMS.
- Experience interacting with service providers or external
business partners
- Excellent teamwork and interpersonal skills are required with
ability to effectively collaborate with internal and external
contacts, building strong sustainable relationships
- Excellent oral and written communication skills, demonstrating
professional maturity, confidence and competence
- Ability to work effectively within a matrix organization to
achieve desired outcomes
- Track record of effective decision-making; makes good business
decisions and analyses problems from multiple perspectives
- Ability to work across cultures, including in a virtual
environment
- Proficiency with MS Office (e.g. Word, Excel, PowerPoint,
Outlook)
- Team Building, Motivating and Influencing Others without
authority
- Promoting Innovation and Process Improvement Maintaining
activities
- Negotiation skills Strong analytical skills Must demonstrate
accountability for delivery of results and have good
problem-solving and decision-making skills
- Must be able to manage their own work, with ability to
prioritize, plan and organize work assignments while working under
strict timelines Jazz Pharmaceuticals is an Equal Opportunity
Employer.
Keywords: Jazz Pharmaceuticals, Philadelphia , Alliance Management Specialist, Pharmacovigilance, Executive , Philadelphia, Pennsylvania
Didn't find what you're looking for? Search again!
Loading more jobs...