Clinical Research Coordinator

We are looking for motivated individuals to join UpTrials, a new online platform that makes it easier and faster to find clinical research jobs. Roles on our site support the coordination and management of clinical research activities and involve working closely with research teams to oversee daily study operations and ensure compliance with all regulatory requirements.

Key Responsibilities:

• Provide guidance and training to clinical research staff.
• Maintain communication with team members regarding study tasks and enrollment.
• Perform clinical tasks such as phlebotomy and monitoring vital signs, as needed.
• Coordinate with external partners, vendors, and suppliers to ensure the availability of study materials.
• Organize and lead regular research meetings.
• Assist with managing day-to-day operations and subject care in clinical research.
• Handle multiple studies: screening, recruiting, scheduling, data collection, and documentation.
• Build and maintain strong relationships with team members and external contacts.
• Ensure compliance with study protocols and regulatory guidelines.
• Support the informed consent process and ensure participant safety.
• Facilitate study-related visits and activities.
• Collect and process laboratory specimens.
• Follow all clinic and sponsor policies and procedures.

Qualifications:

• 1+ years of experience in clinical research coordination.
• Advanced degree or management experience may substitute for one year of required experience.
• Experience in a clinical setting preferred.
• Strong interpersonal and organizational skills.
• Proficiency in MS Office and clinical trial management systems.
• Excellent communication skills.
• Ability to work independently and within a team.
• Willingness to travel as needed for job duties.

Working Conditions:

Applicants must be authorized to work in the U.S. We are unable to sponsor employment visas at this time. This is a full-time position with occasional evening and weekend work required.