Clinical Research Coordinator Lead
Clinical Research Coordinator Lead
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Overview
Responsibilities
Assesses patients for protocol eligibility ensuring the appropriate selection of participants for clinical trials thereby enhancing the accuracy and validity of research outcomes. Confers with study participants to explain the purpose of the study and obtains informed consent fostering transparency and trust with patients and their families throughout the research process.
Collects data from various sources including patient charts medical records interviews and diagnostic tests and prepares comprehensive documentation ensuring the accurate and reliable analysis of research data. When applicable completes documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
Completes clinical tasks (i.e. electrocardiogram (ECG) pulmonary function tests (PFT) phlebotomy drug administration etc. when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
Serves as study coordinator for highly complex trials pharmaceutical and/or device trials successfully coordinating site initiation visits monitoring visits and closeout visits and ensuring adherence to protocol guidelines and regulatory requirements.
Mentors and trains Clinical Research Coordinators I and Clinical Research Specialists I & II to ensure an effective and compliant team. Serves as back up to/supporting role for the Clinical Research Manager assisting with HR support financial support budgeting/contracting support.
Performs other duties as assigned.
Qualifications
Required Experience:
IC
Employment Type
Full-Time
