Clinical Research Associate
Pubblicato il 12-10-2026 - Oxford Global Resources in Montà
Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoring
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- Conduct pre-study visits to assure the site has adequate facilities, staff, and subject population for conducting the study within established time frames
- Coordinate the distribution of supplies to study sites and assure an adequate quantity of supplies on hand during the course of the study
- Track distribution and return of all study materials and drug
- Conduct site initiation in order to ensure that all elements are in place for performing the study according to protocol and in compliance with all applicable regulations and good clinical practice guidelines
- Perform interim site monitoring visits and document findings in a monitoring report which will be completed in a timely manner
- Perform close-out visits to all study sites
- Assist in maintenance of Trial Master Files (TMFs)
- Assist with preparation of informed consent (ICFs), case report forms (CRFs), study support documents for assigned studies
- Review site generated ICFs for compliance with study protocol and federal regulations
- Review and provide feedback to Clinical Trial Team Lead on data management documents
- Review and provide feedback to Clinical Trial Team on pharmacovigilance plans for assigned studies
- Evaluate and recommend selection of investigators/study sites
- Train investigators, coordinator, and other trial staff in data collection methods to ensure collection of patient data that is accurate, complete, and conforms to project data standards and protocol requirements
- Ensure the collection, review, and updating of all essential documents defined by FDA regulations, com