Clinical Research Coordinator 1 - Remote

Overview

The Clinical Research Coordinator (CRC1) is a specialized researcher who supports and coordinates daily clinical trial activities under the direction of the Principal Investigator. This role is crucial in managing compliance, financial, and personnel aspects of clinical studies.

In Short

• Coordinate clinical trial activities from startup to closeout.
• Recruit and screen study subjects.
• Obtain informed consent and collect research data.
• Ensure protocol adherence and manage all aspects of clinical trials.
• Educate patients about study procedures and risks.
• Organize patient schedules for study procedures.
• Maintain accurate records and ensure compliance with regulations.
• Monitor for adverse events during study visits.
• Attend site visits and relevant study meetings.
• Perform other related duties as needed.

Requirements

• College or university degree in a related field.
• Less than 2 years of work experience in a related job discipline.
• Strong organizational and communication skills.
• Ability to interact with clarity and tact.
• Knowledge of Microsoft Word, Excel, and Adobe Acrobat.
• Ability to understand complex clinical trial documents.
• Strong data management skills and attention to detail.
• Adaptability to changing work situations.
• Excellent interpersonal skills.
• Ability to handle competing demands with enthusiasm.

Benefits

• Wide range of benefits programs including health and retirement.
• Paid time off.
• Supportive work environment in a leading research institution.
• Opportunities for professional development.
• Collaborative and innovative team culture.