Clinical Research Coordinator - Yukon, OK

Proclinical Staffing; Yukon (OK); On-site; USD 50,000 - 65,000; Full time

Job summary

A leading life sciences staffing agency seeks a Clinical Research Coordinator in Yukon, OK. In this full-time entry-level role, you will be responsible for managing clinical trial activities, enrolling participants, and ensuring adherence to protocols. The ideal candidate will have a high school diploma and clinical research experience. Strong communication skills and proficiency in English are essential. This position requires cooperation with site staff and management to advance clinical breakthroughs within a collaborative site team.

Responsibilities

• 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 records and logs.
• Schedule study visits and monitor according to protocol.
• Prepare source documents and ensure data accuracy.
• Enter collected data into electronic systems within 48 hours.
• Manage inventory of lab supplies and notify management when needed.
• Perform protocol-specific procedures like vital sign checks.
• Record and report adverse events and resolve data queries.
• Dispense medical devices or drugs and provide instructions.
• Identify and address protocol deviations.
• Participate in quality assurance audits.
• Ensure investigational products are securely stored.
• Maintain confidentiality of patient information.

Skills

Clinical research experience

Ability to work independently and collaboratively

Effective verbal and written communication skills

Proficiency in English

Knowledge of basic medical terminology

Phlebotomy skills

Willingness to travel

Education

High school diploma or GED

Some college or medical certification

Job description

Clinical Research Coordinator - 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

• 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.

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.

Contact Information

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at [e-mail].

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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Seniority level

• Entry level

Employment type

• Full‑time

Job function

• Science

Industries

• Professional Services

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