Clinical Research Coordinator 253251
Medix™
Adhere to clinical trial protocols and coordinate and perform assigned clinical trial activities including, but not limited to:
- Participant pre-screening, recruitment and scheduling
- Complete protocol and trial system training
- Maintenance of regulatory documents
- Conducts or participates in the informed consent process and discussions with trial participants, including answering any questions related to the study.
- Conducting participant visits
- Ability to perform basic lab and clinical procedures per protocol, such as: blood specimen collection (phlebotomy), blood pressure, vitals, EKGs, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up
- Entering data in the EDC and resolving all queries
- Updating and maintaining trial logs and participant charts
Vacancy posted 1 day ago
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