Global Patient Recruitment & Retention Strategy Director

Exelixis Inc; Alameda (CA); On-site; USD 164,500 - 234,500; Full time

Benefits offered by this job

401k plan with generous company"Conrib

Medical, dental and vision coverage

Life and disability insurance

Flexible spending accounts

Discretionary annual bonus program

Long-term incentives stock options

15 accrued vacation days

17 paid holidays

Up to 10 sick days

Job summary

Exelixis Inc. seeks a senior leader to drive recruitment and retention governance for informed consent across global clinical trials. You will align policy with external regulations and collaborate with CROs, vendors, and site teams to meet enrollment goals.

You will guide cross-functional teams, ensure GCP compliance, and manage timelines across programs and therapeutic areas, enabling efficient study execution and staying ahead of industry guidance.

Qualifications

• Leadership and collaboration in complex matrix organizations.
• Ability to think through, provide solutions and innovate to recruit and retain participants for clinical trials.
• Knowledge of regulatory requirements for conducting clinical trials worldwide.

Responsibilities

• Lead the recruitment and retention strategy across informed consent forms and clinical trials.
• Collaborate with CROs, vendors and sites to meet enrollment/retention goals.
• Develop enabling policies aligned with external laws (ICH E6R3).
• Maintain ICH/GCP compliance and quality in informed consent processes.

Skills

Leadership

Cross-functional collaboration

GCP knowledge

Analytical communication

Education

BS/BA in Science or related

MS/MA in Science or related

Equivalent mix of education/experience

Tools

Electronic Data Management

Job description

Exelixis Inc. seeks a senior leader to drive recruitment and retention governance for informed consent across global clinical trials. You will align policy with external regulations and collaborate with CROs, vendors, and site teams to meet enrollment goals.

You will guide cross-functional teams, ensure GCP compliance, and manage timelines across programs and therapeutic areas, enabling efficient study execution and staying ahead of industry guidance.