Job Description

Clinical Research Coordinator - Contract - Yukon, OK

Advance clinical breakthroughs as a Research Coordinator driving excellence in trials and patient care.

Proclinical 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.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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