Executive Director, Clinical Operations

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**:
EXAMPLE RESPONSIBILITIES:

- Provides input into JAPAC regional strategic and operational short
- and long-range therapeutic area / functional area plans as appropriate, including supporting alignment and communications to other team members upon implementation.
- Provides leadership, guidance, oversight and therapeutic expertise for the successful management of all aspects of clinical trials.
- Responsible for the strategic, operational and financial oversight of all program(s) within the region.
- Develops, implements, manages and ensures completion of clinical trials within regional designated budgets and timelines.
- Sets the regional strategic vision for assigned clinical trials / programs by working cross-functionally with all relevant stakeholders.
- Assesses, on-boards and manages regional contract research organizations (CROs) and other vendors to ensure success of assigned trials / programs, including requests for proposals (RFPs) and selection processes.
- Contributes to the regional strategic implementation of Clinical Development Program(s) for specific programs as a member of the Clinical Sub-Team and may sit on the Global Development Team, dependent upon the program’s priority and breadth.
- Oversees regional representation of local Study Management Team(SMT) members and influences relevant stakeholders.
- Performs regional strategic analysis of project status and issues; ensuring robust risk mitigation strategies are in place.
- Anticipates complex obstacles and implements solutions to achieve project goals.
- Solves problems relating to national regulations, guidelines and investigator interactions.
- Keeps all stakeholders appropriately and timeously advised on all aspects of project status and any issues.
- Partners with General Managers within the JAPAC region and other key regional stakeholders to ensure seamless execution.
- Ensures building of strong regional site partnerships (Sponsor of Choice) through management of Clinical Site Partners within the region.
- Uses all available tools to track, oversee and communicate on program status to all key stakeholders.
- Contributes leadership input into all regional study-related documentation, including study protocols.
- Responsible for Clinical Operations activities conducted by the regional affiliates that are required by local regulations and/or usual practice to support clinical trials.
- May contribute to standard operating procedure (SOP) development, implementation and training as it relates to the region.
- Ensures team’s work complies with established practices, policies and processes, and any regulatory or other regional requirements.
- People Leader Path: Hires, develops and retains diverse top talent on the team. Sets clear expectations for the team and individuals direct reports. Coaches direct reports on their performance, development and career interests. May play a central role in developing other people leaders.

REQUIREMENTS:
We are all different, yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.

Minimum Education & Experience
- BA / BS / RN with 14 or more years’ relevant clinical or related experience in life sciences. Or, MA / MS / PharmD / PhD with 12 or more years’ relevant clinical or related experience in life sciences.
- Typically has a minimum of 12 years’ cross-functional study management or related leadership experience in life sciences, including multiple years’ experience managing study management or project teams.
- Experience developing RFPs and selection and management of CROs or other vendors.
- Proven ability to successfully manage clinical studies within designated program budgets and timelines, including significant expertise in authoring clinical study and regulato