Clinical Research Coordinator - Oncology - Contract - Detroit, MI
Are you looking to drive groundbreaking medical research and make a real impact-join our client and lead the way in advancing clinical trials!
Proclinical is seeking a Clinical Research Coordinator to support oncology-focused research projects in Detroit, MI.
Primary Responsibilities:
In this role, you will organise research activities, ensuring compliance with regulatory guidelines and providing technical support to Principal Investigators. This position involves participant interaction, recruitment, and managing the day-to-day operations of multiple studies.
Skills & Requirements:
- Bachelor's degree in a scientific discipline.
- Experience in research project coordination, with a preference for oncology-related studies.
- SOCRA or ACRP certification preferred.
- IATA certification is an advantage.
The Clinical Research Coordinator's responsibilities will be:
- Coordinate research projects while adhering to regulatory compliance and federal regulations.
- Provide technical support to Principal Investigators.
- Oversee recruitment efforts and manage daily study operations.
- Interact with internal and external stakeholders at various levels.
- Maintain direct communication with potential and enrolled study participants.
- Offer additional support as required.
- Manage multiple studies simultaneously.
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.
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