Clinical Research Coordinator
3 weeks ago
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.
Responsibilities
- Perform 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.
Requirements
- At 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
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