
Clinical Research Coordinator
3 hours ago
At PSI CRO, we are committed to supporting clinical trial sites in delivering strong study results. Our team of experts understands the unique challenges that sites face and is dedicated to providing tailored solutions to meet their needs.
Job OverviewThe Clinical Trial Site Coordinator will play a critical role in ensuring the success of our trials. This individual will be responsible for communicating with sponsors and CROs, responding to feasibility questions, and coordinating monitoring visits.
This role requires strong organizational skills, effective communication, and problem-solving abilities. The ideal candidate will have prior experience in coordinating clinical trials and a college degree in a life science field.
We offer a dynamic and supportive work environment, opportunities for professional growth, and a chance to make a meaningful contribution to the development of new treatments.
Key Responsibilities- Act as the main point of contact between sponsors/CROs and trial sites
- Respond to feasibility questions in a timely manner
- Coordinate scheduling and preparation for monitoring visits
- Be present and available to respond to monitors during visits
- Track patient enrollment and support project timelines
- Maintain accurate records and data entry into EDC systems
- Report and follow up on adverse events and protocol deviations
- Handle investigational products and clinical supplies
- Facilitate contract and budget negotiations
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