Clinical Research Coordinator: Impactful Trials 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

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.