Contract Clinical Research Associate, Oncology Sponsor

Category: CRA
Job #: 10947
Utilization: 75%↑
Location: West (or Southwest/Midwest and able to travel to West)
Job Type: 1099
Therapeutics: Hema/Oncology

We're thrilled to share an excellent opportunity with one of our longstanding and most valued Sponsors. They are urgently seeking experienced contract CRAs to support a complex and impactful Hema/Oncology study. Qualified candidates will be located preferably in the Western US and near a major airport. This is a chance to work with a highly respected and stable team while enjoying flexibility and meaningful engagement. If you’re looking to bring your expertise to a Sponsor that values collaboration and excellence in clinical research, this is an exciting project to join. If you meet the requirements, apply below!

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:
  • Must have a minimum of 5 years' recent experience as a fully dedicated Regional, Home-Based, Field Monitor for a CRO or Pharma
  • Must be located preferably in the West US and near a major airport
  • Must have at least 75% utilization available
  • Must have a Bachelor’s degree in any field, or have a medical background
  • At least 2 years' experience monitoring Hema-Oncology is required (experience with Solid Tumor Oncology is a plus)
  • Phase 1 monitoring experience is a plus
  • Must have strong site management skills
  • Must be vaccinated for COVID-19
  • Long-term contract
  • Competitive Hourly Rate
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