Hema/Oncology Partial Contract CRA (Sponsor – Multiple US locations)


Category: CRA
Location: East, MW & SW Regions (US)
Job Type: 1099 (Home-Based)
Rate / Salary Range: 72-80 hourly (USD)

One of our favorite Sponsors has an immediate need to add a couple of CRAs to monitor several Hema/oncology studies.These can be partial contract (you need to have at least 50% utilization available). This Sponsor is extremely flexible and the project is expected to be long term.

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 3 years’ experience as a fully dedicated Regional, Home Based, Field Monitor for a CRO or Pharma; this experience should be recent (i.e. - no longer than 2 years ago.)
  • At least 1 year experience monitoring Hema/oncology projects preferred (other hema/oncology experience in other roles will be considered)
  • Experience monitoring Oncology can be substituted for Hema/Oncology experience
  • Previous experience working with US Oncology and MD Anderson preferred
  • Willing to travel as required to conduct monitoring visits

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