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Sr CRA 2 - FSP - Chicago & Central US

Fortrea
Full-time
Remote friendly (Michigan, United States)
United States
Clinical Research and Development

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Role Summary

Sr CRA 2 - FSP - Chicago & Central US. Experienced Sr. CRAs residing in Chicago and the Central region of the US to join our FSP team.

Responsibilities

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document monitoring data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, e.g. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Requirements

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 4+ years of onsite Clinical Monitoring experience
  • Various therapeutic experience required
  • Open to major hub locations in the Northeast US

Skills

  • Ability to work in a fast-paced environment with strict adherence to study protocol and timelines
  • Strong prioritization and adaptability skills
  • Teamwork and people skills
  • Technology-based environment with data collected electronically

Education

  • Relevant degree or certification as noted in Requirements

Additional Requirements

  • Travel expectations include frequent travel to client sites with occasional domestic and international travel
  • Physical requirements include ability to sit for extended periods, incidental lifting, and ability to operate a vehicle safely
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