- Partner with Principal Investigators (PIs) to guide participants through the informed consent process and conduct ongoing visits, procedures, and assessments.
- Collaborate with PIs to identify and enroll qualified participants for clinical trials, utilizing study portals and various tools.
- Oversee all aspects of trial management, including feasibility assessment, IRB submissions, data collection, quality assurance audits, and regulatory compliance.
- Work with PIs and team members to ensure data quality through independent monitoring and adherence to SOPs, GCP, and regulations.
- Assist in new site startups, study qualification and activation, equipment procurement and installation, ensuring all trial infrastructure is in place.
- BA or BS in health-related field
- Minimum of 3+ years of experience in a research role with an organization involved in conducting industry-sponsored, interventional clinical trials for investigational drugs
- GCP and IATA certification required.
- Spanish speaking skills would be preferable.
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Clinical Research Coordinator - Las Vegas, United States - X4 Life Sciences
Description
An exciting Clinical Site Network are looking to bring on board a Clinical Research Coordinator to either of their sites based out of Las Vegas or Los Angeles.
This role can be offered on either a contract or permanent basis.
The Role:
The Clinical Research Coordinator II is crucial to the companies clinical research, managing multiple complex trials across various areas and phases. Responsibilities include efficient study implementation, participant recruitment, screening, and eligibility determination with the Principal Investigator. As the main contact for participants, sponsors, and regulatory agencies, you ensure clear communication and maintain precise documentation.
Further responsibilities include:
Requirements:
If this could be of interest to you or you would like to learn more, please apply now
