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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As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [email protected] for assistance.
 

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For Current Gilead Employees and Contractors:

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