Hema-Oncology Sponsor Contract Clinical Research Associate SW/W US

Category: CRA
Job #: 10925
Utilization: 100%
Location: Southwest or West US
Job Type: 1099
Therapeutics: Hema-Oncology

We’re excited to highlight a new opportunity with one of our long-standing Sponsors. They are looking for experienced Contract Clinical Research Associates based in the Southwest or West US to oversee sites in CA and TX for cutting-edge Phase I Hema/Oncology studies. This role offers the chance to partner with a stable, well-regarded team while enjoying flexibility and meaningful, hands-on involvement. If you’re ready to contribute your expertise to a Sponsor that truly values collaboration and high-quality clinical research, this could be the ideal next step in your career.

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:
  • Qualified CRAs will have at least 5 years' experience as a fully dedicated regional, home-based, field monitor, having gained that experience from a CRO or Pharma.
  • Must have at least two years' experience monitoring Hema/Oncology studies.
  • Strong experience in monitoring phase I studies required (preferred at least 1 year).
  • Proven track record in site management required.
  • While minimal travel is expected, CRAs must be able and willing to travel as required.
  • Must have at 100% utilization available.
  • Must be located in the Southwest or West US.
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