Director, Product Safety Team Program Management

This position reports into the Office of the Product Safety Team (PST) department within the Pharmacovigilance & Patient Safety Epidemiology and R&D Quality Assurance (PSEQ) organization.
The PSEQ organization works collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand, and communicate the safety profile of our drugs to protect patients worldwide.
The Director, Product Safety Team Program Management plays a critical role in shaping and driving the strategic priorities of Patient Safety through providing exceptional strategic project management leadership across the PST.
The PST is a high-profile, high-impact team that leads and owns safety decisions and strategy across the product lifecycle.
The team partners with stakeholders across the product lifecycle to provide innovative safety-driven strategies, which will maximize product benefit-risk for patients.
This role reports to the leader of the Product Safety Team Program Management organization and supports the leader with people management, project management functions within the PST, and Office of the PST (OOPST) strategic initiatives.
Responsibilities: Provides oversight, leadership, and strategic direction to the Product Safety Team Program Management function within the Product Safety Team (PST), and OOPST strategic initiatives.
Supports the development and implementation of the vision, strategy and objectives of the project management functions within the Product Safety Team (PST), and OOPST strategic initiatives.
Support responsibilities for hiring, coaching, training, onboarding, and managing the performance of PST Program Managers.
Responsible for building and nurturing a culture of strong project management excellence across assigned PM teams.
Builds strong strategic partnerships with all Product Safety Team Program Management stakeholders including Therapeutic Area Heads, PST Leads, BRM and Epi Heads and other stakeholders (within and outside PSEQ).
Seeks their input to shape priorities for the program managers and leverages relationships to advance the goals of the team.
Ensures successful partnership between the assigned program management functions, PST Operational Excellence teams and the PSTs.
Ensures that the assigned PMs are appropriately resourced.
Collaborates with the Product Safety Team Program Management leader to plan and forecast the use of PST PMs across product safety teams.
Seeks creative ways to utilize limited resources and works with Sr.
Director Office of the PST to address critical resource needs.
Responsible for achieving quality and timely metrics for PST and assigned teams.
Collaborates with the Product Safety Team Program Management leader to understand root causes of quality and timeliness issues.
Accountable for ensuring that root causes are addressed within the appropriate PM team.
Partners with the Product Safety Team Program Management leader to define the readiness plan for inspections and audits.
Represents the PST PM team on audit and inspection teams, when required.
Promotes program management best practice and knowledge sharing across Product Safety Team Program Management functions and with other AbbVie program management teams such as the Portfolio Project Managers (PPMs).
Drives assigned critical OOPST leadership initiatives including complex Portfolio Oversight Committee projects that are critical to the success of the PSTs.
Manages Product Safety Teams as assigned.
Represent the PST Lead and PST decisions in committees/meetings.
Supports and coaches PMs in addressing challenges that arise on the PSTs or other project teams, including navigating difficult decisions.
Required Education: Bachelor’s degree in a healthcare discipline (i.
e.
: Life Science, Pharmacy, nursing [associates or equivalent] or healthcare profession, or biomedical disciplines) Preferred Education: Masters or advanced degree is desirable Required Experience: At least 7 years’ experience working in the healthcare industry and a strong understanding of the drug development process.
Experience within Pharmacovigilance is desirable but not required 9+ years hands-on project management experience in leading cross-functional projects within a global matrixed organization.
Hands-on experience applying project management tools and templates Required experience in at least two R&D areas such as clinical study management, regulatory, drug safety, discovery, etc.
Preferred leadership and people management experience.
Experience in directly leading and driving major change initiatives within a team.
Strong leadership presence and demonstrated ability in courageously challenging the status quo and influencing others.
Experience in working directly with and influencing senior management including functional heads High emotional Intelligence and strong relationship management and communication skills Understanding of the connections between regulations and science for the benefit of drug safety Understanding of tools, standards and approaches used to efficiently evaluate drug safety, is desirable but not required AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion.
It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.