Clinical Research Coordinator - Contract - Detroit, MI
Be the link between patients and groundbreaking oncology research-join us as a Clinical Research Coordinator.
Proclinical is seeking a Clinical Research Coordinator to support oncology-focused clinical studies in the US. This position involves participant interaction, study recruitment, and day-to-day operational oversight.
Primary Responsibilities:
The successful candidate will coordinate research projects, ensuring compliance with regulatory guidelines and providing technical support to Principal Investigators.
Skills & Requirements:
- Bachelor's degree in a scientific discipline.
- Experience in research project coordination; oncology experience preferred.
- SOCRA or ACRP certification preferred.
- IATA certification preferred.
The Clinical Research Coordinator's responsibilities will be:
- Coordinate research projects in alignment with regulatory requirements and federal guidelines.
- Provide technical and operational support to Principal Investigators.
- Oversee recruitment efforts and manage daily study operations.
- Maintain direct communication with potential and enrolled study participants.
- Collaborate with internal and external stakeholders at various levels.
- Support multiple studies simultaneously as needed.
If you are having difficulty in applying or if you have any questions, please contact Katlyn Coole at k.coole@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy
