What are the responsibilities and job description for the Contract Clinical Research Coordinator position at Barrington James?
6 Month Contract- Full Time- On Site
We are seeking an experienced and dedicated Clinical Research Coordinator.
This role focuses on managing Vaccine Clinical Trials.
Responsibilities of this role include:
- Coordinate and oversee clinical trial activities in alignment with Good Clinical Practice (GCP) guidelines.
- Manage and conduct clinical trials according to protocols and standards.
- Lead and coordinate all aspects of clinical trials, from startup to data collection and reporting.
- Ensure accurate and compliant documentation practices.
- Communicate effectively with study teams, subjects, sponsors, and vendors.
- Handle supplies from sponsors, including lab kits and investigational products.
- Manage extensive patient enrolment, ensuring high recruitment rates and retention.
- Collaborate with investigators, sponsors, and other stakeholders to maintain protocol compliance.
- Ensure proper handling of biological samples and adherence to IATA certification standards.
- Maintain meticulous study documentation and support monitoring visits.
Requirements:
- Experience in coordinating Vaccine Trials.
- 3 years as a Clinical Research Coordinator or in a similar role.
- Demonstrated success in extensive patient recruitment and enrolment.
- Familiarity with decentralized trial models and associated technologies.
- Certifications:
- Current GCP certification (required).
- Valid IATA certification for biological sample handling (required).
Skills and Competencies:
- Strong organizational and time-management skills.
- Excellent interpersonal and communication abilities.
- Ability to work collaboratively in a fast-paced, multi-disciplinary environment.
- Tech-savvy with knowledge of electronic data capture (EDC) systems and remote trial platforms.
Travel:
Daily commute to clinical site required.
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