**Seeking a full time onsite Clinical Research Coordinator in Marrerro Louisiana 70072**
*MUST be a certified Phlebotomist*
The Clinical Research Coordinator oversees and coordinates the daily activities of
clinical research studies. They work closely with the clinical teams and investigators to
ensure that all required procedures and visits occur according to protocol specific
guidelines.
RESPONSIBILITIES:
• Organize all aspects of the clinical trials assigned.
• Participate in investigator meetings, site initiation meetings, etc. as needed.
• Work with our internal recruitment department for participant screening and
enrollment and ensure compliance with protocol and all applicable regulations.
• Conduct informed consent process and conduct study related visits.
• Monitor subjects per protocol requirements.
• Assess, monitor, and report adverse events per protocol.
• Maintain required records of study activity including source documentation, case
report forms, drug dispensation records, and data management system entry.
• Dispense test articles, calculate dosages if needed, and provide instructions
• Complete case report forms and resolve queries.
• Report protocol deviations to PI, sponsor, and IRB as required.
• Obtain, process and ship study related specimens.
• Provide assistance to fellow study coordinators.
• Manage quality assurance activities for assigned protocols per site SOP’s.
• Ensure adherence to study protocols and study quality, maintains subject
confidentiality.
• All other related duties as assigned.
• Participate in occasional outreach community events
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