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Clinical Research Coordinator I
5 months ago
Participate in recruitment activities to meet enrollment goals. Review medical history to Pre-Screen/Screen/Enroll study participants into clinical trials.Interact with potential study participants to introduce the study and perform the informed consent process.Coordinate, schedule and manage study visits.Conduct study procedures such as blood draws, ECGs, and vital signs.Collect study data and enter it into an electronic data capture system and maintain paper records.Creating data collection documents as needed. Collect study specimens such as blood, urine, etc., process, and ship to designated laboratories. Maintaining study supply inventory and equipment.Communication between study team and sponsors and vendors. Participate in sponsors monitoring visits.Maintain participant study binders.Assist to maintain regulatory documents.
Knowledge, Skills and Abilities:
Ability to communicate effectively with different individuals/groups.Attention to detail.
