Perm Clinical Research Associate

Category: CRA
Job #: 10700
Location: Anywhere US
Job Type: Perm
Therapeutics: Hema/Oncology or Oncology

One of our partners is looking for several Perm CRAs to monitor Oncology and Hema-Oncology Studies. This partner values long term relationships with their CRAs and offers enormous career growth opportunities.

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.
    • Monitor patient enrollment to ensure recruitment targets and project timelines are met at the site and/or country level
    • Act as the main line of communication between the Sponsor and the site
    • Be a point of contact / liaison for in-house support services and vendors
    • Responsible for reviewing the status and contents of essential documents at the site level including reconciliation of the TMF
  • 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 3 years' recent experience as a fully dedicated Regional, Home-Based, Field Monitor for a CRO or Pharma.
  • Can be located anywhere in the US close to a major airport
  • Must have at least one year experience working in either Hema/Oncology or Oncology studies (any role)
  • GI, ID, MS, or Rare Disease monitoring experience is a plus
  • 100% Utilization required

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