Clinical Research Associate

3 days ago


Pittsburgh, Pennsylvania, United States Veterans Health Foundation Full time
Job Overview

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our team at Veterans Health Foundation. As a Clinical Research Coordinator, you will play a vital role in the planning, coordination, and management of clinical trials. This is an excellent opportunity to work with a talented group of medical scientists and make a meaningful contribution to the lives of others through innovative research.

About the Role

The successful candidate will have the opportunity to work on multiple Phase II-IV clinical trials across various disciplines and investigators. You will be responsible for maintaining compliance with all regulatory bodies associated with human subject research. In addition, you will collaborate with Principal Investigators and clinical staff to identify eligible participants for clinical trials and ensure that they are informed prior to obtaining written consent.

You will also be responsible for collecting, maintaining, and storing all relevant clinical data and case report forms in accordance with the study sponsor and all regulatory bodies. Your attention to detail and organizational skills will be essential in ensuring the accuracy and completeness of clinical trial documentation.

Key Responsibilities
  • Study Coordination: Coordinate the initiation, conduct, and completion of assigned clinical trials.
  • Regulatory Compliance: Maintain compliance with all regulatory bodies associated with human subject research.
  • Clinical Data Management: Collect, maintain, and store all relevant clinical data and case report forms in accordance with the study sponsor and all regulatory bodies.
  • Subject Recruitment: Collaborate with Principal Investigators and clinical staff to identify eligible participants for clinical trials.
Requirements

To be successful in this role, you will need to have a strong background in clinical research, including experience in obtaining informed consent, managing clinical trial documentation, and working with electronic medical records. Additionally, you will need to possess excellent communication and interpersonal skills, as well as the ability to work independently and prioritize tasks effectively.



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