Clinical Research Coordinator- Contract - Barrington James

6 Month Contract- Full Time- On Site

We are seeking an experienced and dedicated Clinical Research Coordinator. This role focuses on managing clinical trials, in Women’s Health. The ideal candidate will have a proven track record in patient recruitment, experience with decentralized trials, and a deep understanding of regulatory requirements.

Key Responsibilities:

• Coordinate and oversee clinical trial activities in alignment with Good Clinical Practice (GCP) guidelines.
• Manage extensive patient enrolment, ensuring high recruitment rates and retention.
• Facilitate and monitor decentralized clinical trials (DCTs) across multiple sites.
• 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.
• Support studies in Women’s Health and, as needed, contribute to oncology trials.

Qualifications:

• Required Experience:
• 3+ years as a Clinical Research Coordinator or in a similar role.
• Direct experience in Women’s Health clinical trials.
• Demonstrated success in extensive patient recruitment and enrolment.
• Familiarity with decentralized trial models and associated technologies.
• Preferred Experience:
• Background in oncology clinical trials is a plus.
• 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.