Clinical Research Associate – Opioid (Mid West US)

Category: CRA
Job #: 10565
Location: Midwest US
Job Type: 1099 / Regional Homebased
Rate / Salary Range: Competitive Hourly Rate

One of our partners has a need for multiple Contract CRAs to monitor an Opioid study.  Qualified candidates will have 50% availability and will have at least 3 years of experience working on Opioid Clinical Research studies (in any role).

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 at least 3 years of experience working on Opioid Clinical Research studies (in any role)
  • Utilization: Commitment of at least 50%
  • Long term contract as our client is looking for a long-term relationship with you
  • Competitive hourly rate
  • Must be able and willing to travel as required for monitoring visits

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