Clinical Research Coordinator - St Louis, United States - Medix

Description

Experienced Clinical Research Coordinator (CRC)The CRC is a member of the staff who wants to provide quality, compassionate care to patients while helping research promising new medicines.

The CRC is self-motivated, highly organized, capable of managing multiple projects, and have at least two years of experience in the medical field.

ResponsibilitiesPerform overall data management of studies - collect, enter, and maintain records for clinical study subjects.
Support accurate and timely data entry in electronic databases.
Ensure all protocol-required procedures and visits occur according to specified guidelines.

Manage participant enrollment and ensure compliance with the protocol during participant recruitment, informed consent, participant education, eligibility assessment, participant care, and follow-up per protocol.

Collaborates with quality assurance (QA) in the development of source documentation for new studies, assisting in the assessment of toxicities/adverse events and reporting serious adverse events per IRB and sponsor requirements.

Possess excellent interpersonal skills and collaborative with the research team.
Independently manage workflows and prioritize numerous tasks.
Be flexible and anticipate time-frames to accommodate frames subjects, monitors, and overtime hours during high-enrolling study periods.
Maintains GCP certification and IATA training as required.
Performs other duties as assigned.
RequirementsAt least two years of experience as a clinical research coordinator.
Excellent oral and written communication skills.
Demonstrated ability to work well independently and with subordinates.
Demonstrated ability to manage frequent deadlines and competing priorities.
Computer proficiency.
Critical thinking and analytical skills