Gilead Sciences

Executive Director, Project Management - Virology

Posted on: 16 Jan 2021

Foster City, CA

Job Description

Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensure the health and safety of our teams.

For Current Gilead Employees and Contractors:

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

Job Description



Position Overview:

The Executive Director of R&D Project Management partners with the Therapeutic Area (TA) Leader for Virology to coordinate TA level activities, including running the TA cross-functional Leadership Team. The leader ensures that the programs within the TA are moving at the required cadence and in line with Gilead governance and company goals and that programs are adequately staffed. In addition, this leader ensures that the programs have timely governance oversight for their required decisions as well as mentors, guides and provides development opportunities for a team of 3-5 Project Managers at various levels.

Key Responsibilities:

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

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

* Facilitates goal-setting at the TA level, ensuring alignment with company goals

* Aligns on agenda items for Governance and seeks decision from Governance in a time-appropriate fashion

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

* Liaises with Development, Research and Commercial to facilitate alignment on strategy and project priorities

* Works with TA head & VP Project Management to appropriately assign project leads and project managers for a given program

* Due Diligence participates in assessing and reviewing potential opportunities; provides integration; and project management support postacquisition

* Ensures project management attendance at all Research Scientific Project Reviews pertaining to their projects and be the conduit to Research for the development support required to support governance approval for the transition of a molecule between Research & Development

* 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 Scientific Advisory Boards and the Portfolio Review process

Minimum Qualifications:

* Bachelors degree with 15+ years OR Masters degree with 12+ years OR PhD 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

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


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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 careers@gilead.com for assistance.

For more information about equal employment opportunity protections, please view the EEO is the Law poster.

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Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

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

Gilead Sciences

Foster City, CA

Gilead Sciences, Inc., a research-based biopharmaceutical company, discovers, develops, and commercializes medicines in the areas of unmet medical needs in the United States, Europe, and internationally. The company’s products include Biktarvy, Descovy, Odefsey, Genvoya, Stribild, Complera/Eviplera, Atripla, and Truvada for the treatment of human immunodeficiency virus (HIV) infection in adults; and Vosevi, Vemlidy, Epclusa, Harvoni, and Viread products for treating liver diseases.

It also provides Yescarta, a chimeric antigen receptor T cell therapy for adult patients with relapsed or refractory large B-cell lymphoma; Zydelig, a kinase inhibitor; Letairis, an oral formulation of an endothelin receptor antagonist for pulmonary arterial hypertension; Ranexa, a tablet to treat chronic angina; and AmBisome, an antifungal agent to treat serious invasive fungal infections. In addition, the company offers its products under the name Cayston, Emtriva, Hepsera, Sovaldi, and Tybost. Further, it develops product candidates for the treatment of HIV/AIDS and liver diseases, hematology/oncology, inflammation/respiratory diseases, and others.

The company markets its products through its commercial teams; and in conjunction with third-party distributors and corporate partners. Gilead Sciences, Inc. has collaboration agreements with Bristol-Myers Squibb Company; Janssen Sciences Ireland UC; Japan Tobacco Inc.; Galapagos NV; Scholar Rock Holding Corporation; Tango Therapeutics; National Cancer Institute; Pfizer, Inc.; Sangamo Therapeutics, Inc.; Gadeta B.V.; HiFiBiO Therapeutics; Agenus Inc.; HOOKIPA Pharma Inc.; Goldfinch Bio, Inc.; and insitro Inc. The company was founded in 1987 and is headquartered in Foster City, California.

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