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Sr. Clinical Research Associate

Organization
Beaufort, LLC
Job Location
999 Waterside Dr.
Norfolk, VA 23510
United States
Salary
Negotiable
Job Description

Beaufort is currently looking for a full time Clinical Research Associate (CRA) to join our team! We are looking for a dynamic and hardworking CRA that is interested in being in the cutting edge industry of in-vitro diagnostics. This CRA will have the ability to work with multiple sponsors in multiple therapeutic areas and indications. This is a remote position, working from home-office, with travel to site locations nationwide required.

  • Ensure data quality and compliance with protocol, SOPs, and regulations at assigned study sites.
  • Monitor patient recruitment timelines at sites and report this information to assigned line manager.
  • Assist with the arranging of study start-up meetings if necessary.
  • Understand the protocol and therapeutic area in sufficient detail to be able to advise and discuss with the study site personnel.
  • Conduct site selection activities including site selection visits if necessary.
  • Perform site qualification visits, initiation visits, interim monitoring visits, and close-out visits as necessary.
  • Write and review case report forms if necessary.
  • Responsible for checking supplies and site compliance with protocol and all current and relevant regulations.
  • Responsible for conducting source data verification and providing written follow-up requests to the site in order to correct any issues identified at the monitoring visit.
  • Write and submit site visit reports per specified timelines and guidelines.
Requirements
  • Bachelor's Degree required, preferably in a scientific related field.
  • Must have at least 2-3 years' experience as a field monitor CRA.
  • Experience monitoring IVD studies required.
  • Must have full home office capabilities.
  • Must have excellent oral and written communication skills.
  • Must have the ability to be flexible and change priorities quickly.
  • Must be able to strictly follow ICH/GCP guidelines, SOPs, and meet all deadlines.
  • Must be able to travel up to 75%.
How to Apply

Please send a copy of your resume to: lpettrey@beaufortcro.com 

About Our Organization

Beaufort is a leading Diagnostic Contract Research Organization (CRO) offering consulting services to Medical Device, In Vitro Diagnostics, Biologics, and Pharmaceutical companies in the areas of Clinical Trial Management, Quality Assurance, and Regulatory Affairs. Beaufort offers a competitive salary and benefits package. For more information, please visit our website at www.BeaufortCRO.com. 

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