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Sr CRA - Oncology - FSP - North Central & West Coast

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

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Role Summary

Sr CRA - Oncology - FSP - North Central & West Coast. Experienced Oncology CRAs residing in the North Central (IL, MN, MO, IA, KA) or West Coast (CA, AZ).

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, eg. 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

Qualifications

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

Skills

  • Fast paced work environment with strict adherence to protocol
  • Ability to adapt to changing priorities
  • Strong teamwork and people skills
  • Technology-based data collection in an electronic environment

Education

  • Not specified in the provided content

Additional Requirements

  • Frequent travel to client sites with occasional domestic and international travel
  • Physical requirements: see provided list (sitting, lifting up to 15–20 lbs, manual dexterity, etc.)