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Clinical Research Coordinator
2 months ago
We are seeking a highly skilled Clinical Research Coordinator to join our team at Common Spirit. As a Clinical Research Coordinator, you will play a critical role in ensuring the successful conduct of clinical trials and studies.
Key Responsibilities- Ensure compliance with regulatory requirements, including FDA, OHRP, and IRB guidelines.
- Recruit and screen potential participants for clinical trials.
- Coordinate with investigators to obtain informed consent and enroll participants in studies.
- Perform various procedures, including laboratory tests, phlebotomy, vital signs, ECG, and outcomes assessments.
- Obtain medical history and medical records as required by study protocols.
- Respond to patient inquiries in a timely manner.
- Process and ship laboratory samples as outlined in study protocols.
- Provide participant education on study procedures, proper dosage, and specific restrictions.
- Complete case report forms, data entry, and maintain source documentation for all study participants.
- Prepare for participant visits, including scheduling and source document creation.
- Triage, track, and report adverse events and deviations to the investigator and sponsor.
- Coordinate research monitor visits and respond to data queries in a timely manner.
- Minimum 2 years of related experience required.
- Competent in computer skills, including Microsoft Office products.
- Associates degree in a related field or an equivalent combination of relevant education and/or job-related experience in lieu of degree required.
- Three (3) years of clinical research experience preferred.
- Bachelors degree in a related field preferred.
