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
The role covers site identification and qualification, enrollment planning and execution, timely database lock, and study closeout.
The position serves as a communication bridge and escalation point between investigator sites and the Development organization, working with internal teams and site staff to resolve issues and remove barriers.
The position also manages relationships with regional and local patient advocacy groups and communities to ensure that the patient perspective is incorporated throughout product development.
- Establish and maintain strong professional and collaborative relationships with investigator sites, leveraging disease area expertise to optimize clinical trial delivery.
- Develop strategies to provide high-touch support for preferred sites and strengthen the company’s position as a sponsor of choice.
- Track key performance metrics to assess site performance and identify opportunities for and continuous improvement.
- Maintain therapeutic and technical expertise to enable scientific discussions with investigators and site personnel.
- Share development pipeline information with investigators/site personnel and collect field-based intelligence on the competitive landscape, patient pathways, and operational considerations.
- Support study teams and CROs to deliver trials from initiation through closeout, including feasibility, site recommendations, initiation visits, communication facilitation, and enrollment support.
- Support the development and implementation of site risk plans to achieve key study and site milestones such as first patient first visit, enrollment commitments, and database lock.
- Serve as a local escalation point for investigator sites, partnering with appropriate stakeholders to resolve issues and remove barriers at site and/or country level.
- Proactively communicate and escalate site issues, and partner with internal functional areas to develop mitigation strategies and implement solutions.
- Leverage and present metrics to inform site, country, and regional decision-making.
- Develop local knowledge of site capabilities and past performance and provide input into recruitment forecasts and methodologies while monitoring performance and taking action to maintain timelines.
- Partner closely with Clinical Operations, Clinical Development, and Medical Affairs to ensure effective communication and unified messaging to investigator sites.
- Therapeutic Area: Oncology, Virology and Inflammation disease
Required Qualifications:
5+ years of Clinical Operations experience in a pharmaceutical company, biotech, or CRO
Hands-on experience managing clinical trials from start-up through closeout
Strong investigator site relationship management and engagement experience
Experience with site feasibility, site selection, site activation, and enrollment support
Proven ability to resolve site issues and manage escalations
Strong understanding of ICH-GCP and local clinical trial regulations
Experience using KPIs and performance metrics to drive trial execution
Therapeutic area expertise in Oncology, Virology, or Inflammation/Immunology
Ability to collaborate effectively with Clinical Operations, Clinical Development, Medical Affairs, and CRO partners
Strong communication and stakeholder management skills
Business-level English proficiency and native-level Japanese proficiency
Preferred Qualifications:
Experience as a Clinical Site Partner, Site Engagement Lead, Site Partnership Manager, or similar role
Oncology clinical trial experience, particularly in complex or global studies
Experience with patient recruitment acceleration and enrollment recovery initiatives
Experience developing site risk mitigation and performance improvement strategies
Experience working with Patient Advocacy Groups (PAGs) or patient communities
Global clinical trial experience within a matrix organization
Experience leveraging site and country-level metrics to support strategic decision-making
Established relationships with key investigator sites and KOLs
Experience collaborating closely with Medical Affairs and MSL teams
Advanced degree in Life Sciences, Pharmacy, Nursing, or a related field
For Current Gilead Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.
Sign in
To continue your applicationor continue with email
By continuing you agree to our Terms & Privacy Policy.
