ExelixisHiring

Patient Recruitment and Retention Strategy and ICF Governance Director

  • Remote, worldwide
  • Lead
  • Posted 4 days ago
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In one line

Director role leading recruitment and retention strategy and informed consent governance across clinical trials in oncology and other areas, working with study teams, CROs and sites.

About the role

The position spans all programs, phases and therapeutic areas, setting policy and targets for enrollment and for reaching under-represented groups. Informed consent templates and reviews sit under this role, with compliance to global rules as the measure of good work.

At a glance

Pay
Not stated in the posting
Remote scope
Remote, worldwide
Seniority
Lead
Skills
ICH E6R3, ICH/GCP, Informed consent, Clinical trials, Electronic data management
Posted
25 Oct 2026
Last checked
28 Oct 2026

What you will do

  • Run recruitment and retention methodology across the portfolio within budgets and timelines
  • Lead the cross-functional informed consent governance team and its reviews
  • Update generic consent templates to match current global guidance and requirements
  • Train CROs on internal processes and templates and keep ICH/GCP compliance
  • Build tactics with stakeholders to hit enrollment goals, including patient-friendly documents
  • Gather consent submission data into a repository to speed up study timelines

What they look for

  • BS/BA in science, business or related field plus at least 13 years of related experience, or MS/MA plus 11 years, or equivalent
  • At least 6 years working with global informed consent processes and forms
  • Experience across tumor indications and trial phases, and with electronic data management
  • Knowledge of GCP and worldwide regulatory requirements for clinical trials
  • Leadership in complex matrix organizations and skill at reducing patient and site burden

Nice to have

  • Close working relationships built with trial sites

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Questions about this job

Is this a remote job, and where can I work from?

Yes, it is listed as remote, and the posting does not tie it to one country.

What does this job pay?

No pay range is stated in the posting.

What experience is needed?

It is a lead role. The posting asks for: BS/BA in science, business or related field plus at least 13 years of related experience, or MS/MA plus 11 years, or equivalent; at least 6 years working with global informed consent processes and forms; experience across tumor indications and trial phases, and with electronic data management. Skills it names include ICH E6R3, ICH/GCP, Informed consent, Clinical trials.

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