Clinical Trials Director

5 days ago


Birmingham, Birmingham, United Kingdom Tilda Research Inc. Full time

Tilda Research Inc. is accelerating the development of new medical treatments by providing easy access to clinical trials. As a tech-enabled clinical trial network, we build software and services to help pharma innovators execute their clinical trial programs.

We operate a growing network of clinical research sites in the US, with expertise in over 250 pan-indication Phase I through IV studies. Our team also builds software and supports clinical trial infrastructure to identify, enroll, and execute clinical trials efficiently.

Our organization seeks an experienced Psychiatrist to oversee our studies, responsible for ensuring successful execution of research protocols, patient safety, compliance with regulatory requirements, and contributing to our research site's growth and success.

Key Responsibilities:
  • Provide overall medical direction and review of protocols in accordance with the investigational plan and good clinical practice.
  • Assess the medical and scientific feasibility of new sponsor inquiries.
  • Ensure participant safety and well-being at the trial site.
  • Verify data credibility and accuracy collected at the study site.
  • Participate in monitoring visits and sponsor meetings; allow monitoring and auditing by sponsors and inspection by regulatory agencies.
  • Review participants' medical history.
  • Maintain accurate, complete, legible, and timely data reported on the CRF and consistent with source documents.
  • Inform participants about trial termination or suspension and provide appropriate therapy and follow-up.
  • Report Serious Adverse Events (SAEs) or any abnormalities affecting participant safety to sponsors and the IRB according to specific guidelines.
  • Ensure study documents are approved by the IRB and comply with GCP and other regulatory requirements.
  • Maintain trial documents as specified by the Essential Documents section of the ICH guidelines and applicable regulatory requirements.


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