Clinical Research Coordinator - Contract - Yukon, OK
Advance clinical breakthroughs as a Research Coordinator driving excellence in trials and patient care.
À±½·ÊÓƵ is seeking a Clinical Research Coordinator to join a collaborative site team in Oklahoma. This position involves direct communication with site staff, management, and study participants, as well as adherence to standard operating procedures (SOPs).
Primary Responsibilities:
The successful candidate will be responsible for the daily operations and management of assigned clinical trials, ensuring compliance with protocols and regulatory requirements.
Skills & Requirements:
- Clinical research experience preferred.
- Ability to work independently and collaboratively within a team.
- High school diploma or GED required; some college or medical certification preferred.
- Effective verbal and written communication skills.
- Proficiency in English (reading, writing, speaking).
- Knowledge of basic medical terminology.
- Phlebotomy skills if required by state law.
- Willingness to travel to assist or train at research sites as needed.
The Clinical Research Coordinator's responsibilities will be:
- Enroll participants in clinical trials according to protocols.
- Inform patients or caregivers about studies and associated procedures.
- Monitor study activities to ensure compliance with protocols and regulations.
- Maintain and manage study e-regulatory binders and training logs.
- Schedule study visits and monitor schedules per protocol and study plan.
- Prepare source documents prior to participant visits and ensure accurate data collection during visits.
- Enter collected data into electronic data capture (EDC) systems within 48 hours of visits.
- Manage inventory of lab and study supplies, notifying management when restocking is needed.
- Maintain records of study activities, including case report forms and drug dispensation logs.
- Perform protocol-specific procedures such as taking vital signs, conducting electrocardiograms, and collecting laboratory specimens.
- Record and report adverse events, resolving data queries promptly.
- Dispense medical devices or drugs, calculate dosages, and provide instructions as required.
- Identify and address protocol deviations or unanticipated events.
- Participate in quality assurance audits and study initiation visits (SIVs).
- Ensure investigational products are stored securely and maintain accurate logs.
- Maintain confidentiality of patient and sponsor information.
- Perform other duties as assigned.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
À±½·ÊÓƵ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓƵ is acting as an Employment Agency in relation to this vacancy.
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