Perm Clinical Research Associate, Oncology

Category: CRA
Job #: 10957
Utilization: Perm
Location: From Colorado to West
Job Type: Perm
Therapeutics: Oncology

We are looking for experienced CRAs to join one of our favorite partners in a permanent role on an oncology study. This is a global, quality-driven organization where CRAs are supported by leadership that wants to see them grow. Management is accessible, the team works together instead of in silos, and people enjoy coming to work...the kind of place where you can build a long-term career instead of just filling a seat.

The sites are in Colorado, California, Arizona, and Utah, so we are looking for CRAs based anywhere from Colorado to the West Coast. The work is a mix of remote and onsite monitoring with about 50 to 75% travel. Apply below to start the conversation with our team.

Job Responsibilities:
  • Act as the "Site Manager" ensuring relationship with site(s) are positive, issues are resolved quickly, and communications are strong across all verticals.
  • Assist with the development of study manuals, CRFs, monitoring standards, site study tools and other study materials as required.
  • Develop and implement site recruitment, selection and initiation plan.
  • Manage and drive patient recruitment and enrollment tracking.
  • Provide training to sites on the study protocol, study conduct, CRF completion, and data management expectations.
  • Ensure essential document collection for completeness per regulatory requirements.
  • Serve as a liaison with Investigators, Institutions, and sites to provide support during the conduct of the clinical trial and serve as a resource for protocol and procedures.
  • Demonstrate knowledge of on-site monitoring to ensure compliance with GCPs, study protocols, and SOPs.
  • Manage one or multiple studies.
  • Monitor product supplies/accountability, including proper storage, dispensation, and disposal.
  • Manage study completion activities, including CRF collection, query resolution, record archiving, and site closeout activities.
  • Review in-house data and study tables.
  • Mentor, coach, and provide guidance to clinical staff as appropriate.
  • Supervise and train other employees as appropriate.
Job Qualifications:
  • Minimum of 5 years of experience as a fully dedicated regional/home-based field monitor for a CRO or pharma, with active experience within the last 2 years
  • At least 2 years of Oncology monitoring experience
  • Bachelor's degree from an accredited North American institution
  • Located anywhere from Colorado to the West Coast, with no travel restrictions and proximity to a major airport
  • Must be able to travel 50-75%
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