ONSITE - NOT REMOTE

Summary:

The Clinical Research Coordinator I (CRC I) supports the coordination and execution of clinical research studies while developing foundational skills in protocol implementation, participant coordination, and research operations. This role is designed as a developmental position within the research career pathway. CRC I staff work collaboratively with senior coordinators and research leadership while progressively building independence, clinical research knowledge, and problem-solving ability. The CRC I contributes to safe participant care and accurate study execution while developing toward independent study ownership.

Duties:

Study Coordination Support

• Coordinate participant scheduling and protocol-required visits
• Assist with study-related documentation and data collection
• Maintain accurate source documentation under guidance
• Support study start-up and ongoing study activities Participant Coordination
• Communicate with participants regarding study visits and follow-up
• Assist with participant screening processes
• Support participant retention and visit compliance
• Escalate clinical or protocol concerns appropriately Documentation & Data Responsibilities
• Maintain complete and accurate study records
• Assist with data entry and verification
• Prepare documentation for monitoring visits and review
• Follow protocol and regulatory requirements consistently Team Collaboration
• Work closely with

CRC II/III

staff, regulatory personnel, and clinical teams

• Participate in team problem-solving discussions
• Ask questions and seek clarification when appropriate Professional Development
• Develop understanding of research protocols and GCP principles
• Build organizational skills and clinical research knowledge
• Progress toward independent ownership of studies Growth & Development Pathway Growth within the CRC I role includes:
• Increasing comfort with protocol requirements
• Improved organization and documentation skills
• Growing ability to anticipate study needs
• Developing confidence in participant coordination Potential future pathways include:
• Advancement to CRC II with demonstrated independent study management
• Expanded responsibility within assigned research areas

Pay:

$25.00 - $27.00 per hour Expected hours: 40.0 per week

Benefits:

401(k) Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Retirement plan Vision insurance

Education:

Bachelor's (Required)

Experience:

Clinical Research:

3 years (Required)

Location:

Buffalo, NY 14221 (Required)

Work Location:

In person