Foster City, California, USA
1 day ago
Executive Director, Global Program Management (Pharma)
For Current Gilead Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

Position Overview:

The Executive Director of Global Program Management provides key leadership within the GPM organization and across the representative Therapeutic Area (TA). This position could be responsible for either the Oncology or Inflammation TA, both of which are critical to the continued diversification of Gilead’s portfolio. The leader partners with Therapeutic Area (TA) Leaders to coordinate TA level activities, including managing the book of work and TA-level governance reviews. The leader ensures that the programs are moving at the expected cadence, that they operate in line with Gilead governance and company goals, and that they are adequately staffed. The leader is a key member of the GPM leadership team, which is responsible for driving excellence in project management across the portfolio. In particular, the leader mentors, guides and provides development opportunities for a team of 4-8 Project Managers at various levels.

Key Responsibilities:

Leads, coaches and develops a team of Project Managers/Leaders at various career levels aligned to the therapeutic area

Directs highly complex project communications at the executive level and ensures that all TA stakeholders are fully informed and knowledgeable of project activities and their status

Supports the team system, fostering connections between teams, functions, and governance

Schedules, coordinates preparation for and manages TA governance meetings in partnership with TA leaders

Ensures pre-read content for Governance is complete with the required cross-functional input and fit with TA strategy

Facilitates goal setting at the TA level, ensuring alignment with company and program goals

Liaises with Development, Research, Commercial, and Program Strategy Leadership to facilitate alignment on strategy and project priorities

Works with TA Leaders & VP Project Management to appropriately resource programs according to priority and team structure

Due Diligence – participates in assessing and reviewing potential opportunities; provides integration and project management support post–acquisition

Facilitates smooth transition of a molecule between Research & Development through clarity of portfolio priority, team resourcing, and roles and responsibilities

Provides updated TA level documents and information for quarterly consolidated R&D updates, R&D LE budget reviews, quarterly investor relations/Board of Director updates, the Portfolio Review process, and other required reporting

Minimum Qualifications:

Bachelors degree with 16+ years OR Masters degree or PhD with 14+ years in a scientific discipline/DVM/MD with 10+ years of project management and pharmaceutical line management and/or pharmaceutical functional area scientific experience

Previous experience participating in cross-functional project management at the Therapeutic Area level

Extensive understanding of and experience guiding Project Teams through the drug development process

Extensive understanding of and application of principles, concepts, practices, and standards of pharmaceutical project management

Ability to understand and communicate scientific and business elements associated with the therapeutic area(s) of assigned projects at the executive level interpersonal, organizational, and written and verbal communication skills.

Prior people leadership experience

Proven ability to work successfully in a team-oriented, highly-matrixed environment

Proven experience successfully supporting multiple complex, time-sensitive activities simultaneously

Advanced knowledge and skill with Microsoft Project, Microsoft Excel and other reporting and tracking tools. Planisware experience is preferred.

Ability to work successfully under minimal (at times, no supervision), determine personal work plan, and operate independently

Key Responsibilities:

Leads, coaches and develops a team of Project Managers/Leaders at various career levels aligned to the therapeutic area

Directs highly complex project communications at the executive level and ensures that all TA stakeholders are fully informed and knowledgeable of project activities and their status

Supports the team system, fostering connections between teams, functions, and governance

Schedules, coordinates preparation for and manages TA governance meetings in partnership with TA leaders

Ensures pre-read content for Governance is complete with the required cross-functional input and fit with TA strategy

Facilitates goal setting at the TA level, ensuring alignment with company and program goals

Liaises with Development, Research, Commercial, and Program Strategy Leadership to facilitate alignment on strategy and project priorities

Works with TA Leaders & VP Project Management to appropriately resource programs according to priority and team structure

Due Diligence – participates in assessing and reviewing potential opportunities; provides integration and project management support post–acquisition

Facilitates smooth transition of a molecule between Research & Development through clarity of portfolio priority, team resourcing, and roles and responsibilities

Provides updated TA level documents and information for quarterly consolidated R&D updates, R&D LE budget reviews, quarterly investor relations/Board of Director updates, the Portfolio Review process, and other required reporting

Minimum Qualifications:

Bachelors degree with 16+ years OR Masters degree or PhD with 14+ years in a scientific discipline/DVM/MD with 10+ years of project management and pharmaceutical line management and/or pharmaceutical functional area scientific experience

Previous experience participating in cross-functional project management at the Therapeutic Area level

Extensive understanding of and experience guiding Project Teams through the drug development process

Extensive understanding of and application of principles, concepts, practices, and standards of pharmaceutical project management

Ability to understand and communicate scientific and business elements associated with the therapeutic area(s) of assigned projects at the executive level interpersonal, organizational, and written and verbal communication skills.

Prior people leadership experience

Proven ability to work successfully in a team-oriented, highly-matrixed environment

Proven experience successfully supporting multiple complex, time-sensitive activities simultaneously

Advanced knowledge and skill with Microsoft Project, Microsoft Excel and other reporting and tracking tools. Planisware experience is preferred.

Ability to work successfully under minimal (at times, no supervision), determine personal work plan, and operate independently


 

The salary range for this position is: $274,635.00 - $355,410.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


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For Current Gilead Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.

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