Bring a strong understanding of GCP, ICH, and knowledge of regulatory requirements in support of
Adhere to the Code of Federal Regulations (Title 21) and guidelines set up by the International
Oversee and manage the timely closure of queries issued to clinical trial investigator sites and/or
Work with the CTM to proactively identify trends and provide feedback to internal departments
Monitor the performance of both the Investigator(s) and/or the Laboratory as applicable.
Monitor study specific and/or Sponsor requested requirements.

🎯 Requirements

3+ years of clinical research experience in medical device and/or drug development clinical trials.
BS or BA in a relevant scientific discipline.
Good organizational skills, attention to details, and ability to multitask.
Experience in digital pathology, radiology or other imaging technology-based clinical trials is
Project Management Certification is a plus.

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