Clinical Research Coordinator - System One
Overview
Join a busy onsite clinical research site in Dallas, TX as a Clinical Research Coordinator supporting vaccine and other clinical trials. You will coordinate study visits assist with informed consent maintain source documentation and ensure compliance with GCP SOPs. Partner with the PI research staff and participants to drive quality and patient experience.
What You'll Do11
- 1Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff
- 2Conduct screening visits to collect medical history and other information from study participants
- 3Support informed consent and enrollment of study participants according to protocol requirements and ethical guidelines
- 4Coordinate and schedule study visits procedures and follow-up activities with participants and clinical teams
- 5Collect record and maintain accurate clinical research data and source documentation in compliance with regulatory standards
- 6Communicate with participants to provide education answer questions and support adherence to study requirements
- 7Monitor study progress and report adverse events protocol deviations and other issues to the research team
- 8Adhere to site standard operating procedures and Good Clinical Practice guidelines
- 9Draw process and ship laboratory specimens handling dangerous goods as qualified
- 10Scan upload file and maintain organized study records applying critical thinking to resolve problems
- 11Perform other duties as assigned
Requirements12
- 1High school diploma or equivalent required with an associate’s degree or higher in a health-related field preferred
- 2Basic knowledge of clinical research strongly preferred
- 3Medical terminology and patient care experience required
- 4Strong organizational time management and attention-to-detail skills with ability to manage multiple priorities
- 5Ability to communicate clearly and professionally with diverse populations
- 6Ability to work collaboratively in a fast-paced team-oriented environment
- 7Knowledge of GCP HIPAA ALCOA principles FDA regulations and IATA guidelines strongly preferred
- 8Experience with participant screening and the informed consent process strongly preferred
- 9Proficiency with electronic data capture systems clinical trial management software and Microsoft Office applications
- 10Medical Assistant certification preferred
- 11Current CPR/BLS certification preferred
- 12Certification as a Clinical Research Coordinator such as CCRC or willingness to obtain it
Salary Insight
$26 - $30k per year
Location
Required Skills
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