Contract Clinical Research Coordinator

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.