Contract to Perm Clinical Research Associate (Eastern US Time Zone)


Category: CRA
Job #: 10692
Location: Eastern US Time Zone
Job Type: Contract to Perm
Rate / Salary Range: Competitive Rate/Salary

One of our sponsor partners has an immediate need for a CRA in the Eastern US (Eastern Time Zone) to begin as a Contractor with conversion to Perm within 6 months. A minimum of 1 years' experience in Device studies is required with virtual presentation experience in speaking with your employer’s team, investigators and site support staff.  A Bachelor’s degree in a scientific or health-related field is required, and you must have 100% utilization available.

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 3 years' recent experience as a fully dedicated Regional, Home-Based, Field Monitor for a CRO or Pharma
  • Minimum of 1 years' experience in Device studies
  • Cardiac and clinical writing experience is a plus
  • Must have virtual presentation experience in speaking with your employer’s team, investigators and site support staff
  • A Bachelor’s degree in a scientific or health-related field is required
  • Must have 100% utilization
  • Must be located in the Eastern Time zone

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