Clinical Research Associate

4 weeks ago


King of Prussia, Pennsylvania, United States ACL Digital Full time

Clinical Research Associate Role at ACL Digital

The Clinical Research Associate is a key member of our team at ACL Digital, responsible for ensuring the successful execution of clinical trials. This includes site initiation, monitoring, and close-out of clinical trial sites. Our team works on various phases of clinical trials, from Phase 1 to Phase 4.

  • Monitor activities conducted by clinical investigative sites to ensure compliance with federal regulations, Good Clinical Practices (GCPs), and quality standards.
  • Verify subject safety and protect the confidentiality and well-being of study subjects.
  • Conduct site qualification, site initiation, interim monitoring, and close-out visits for clinical trials.
  • Verify completeness, accuracy, consistency, and compliance of trial data collected at study sites.
  • Complete monitoring reports and follow-up letters, providing summaries of significant findings and recommended actions.

Requirements

  • Bachelor of Science Degree
  • 4-5 years of experience with a Sponsor or CRO
  • Site monitoring experience
  • Experience with set-up monitoring plan, conducted site monitoring, and conducted site close-out
  • Medical Device preferred, Pharma OK, CRO OK


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