4 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 enrollment, 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 enrollment.
- 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.