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Ophthalmology & Biopharma - CRA II & Sr. CRAs

Fortrea
Full-time
On-site
United States
Clinical Research and Development

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Role Summary

Ophthalmology & Biopharma CRA II & Sr. CRAs needed to lead and support a Full Service Outsourcing team. Open to major hub locations on the East & West Coast. 60-70% travel, 8-10 DOS per month.

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)
  • 1 - 3+ years of Clinical Monitoring experience
  • Ophthalmology experience is desired
  • Open to various hub locations

Skills

  • Ability to work in a fast-paced environment with strict adherence to study protocol and timelines
  • Adaptability to changing priorities
  • Teamwork and strong people skills
  • Technology-driven environment with data collected electronically

Education

  • Not specified beyond degree/certification requirements in Qualifications

Additional Requirements

  • Travel: 60-70% travel, including domestic and international as needed