Clinical Research Coordinator (Part-Time) - Remote

Overview

The Clinical Research Coordinator I oversees and administers research study and associated activities, ensuring compliance with study protocol and regulatory requirements.

In Short

• Oversee research study and ensure compliance with protocols.
• Assist in project planning and coordination.
• Recruit and coordinate research subjects.
• Maintain record keeping systems and procedures.
• Ensure safety and confidentiality of research participants.
• Plan and implement data collection systems.
• Coordinate day-to-day activities of support staff.
• Document all correspondence related to research.
• Interact with Principal Investigator and other personnel.
• Comply with applicable rules and regulations.

Requirements

• Bachelor's degree or equivalent work experience required.
• 2-4 years experience in clinical research preferred.
• Strong oral and written communication skills.
• Organized and detail-oriented.
• Proficient with Microsoft Office, especially Excel.
• Knowledge of CFR, GCP, and ICH guidelines.
• Flexible with changing priorities.
• Professional demeanor.
• Experience in non-profit or healthcare desired.
• Ability to perform basic study-related procedures.

Benefits

• Competitive medical, dental, and vision healthcare.
• Flexible Spending Account and Health Savings Account.
• Short- and long-term disability insurance.
• 403b retirement plan with employer match.
• Flexible leave options and 11 paid holidays.
• Up to 4 weeks of paid time off per year.
• Employee Assistance Program.
• Qualify for PSLF as a nonprofit organization.
• Benefits vary for part-time positions.
• Equal opportunity employer.