Overnight Clinical Research Coordinator - Study Execution

Taleo; Pittsburgh (Allegheny County); On-site; USD 52,000 - 78,000; Full time

Job summary

The University of Pittsburgh's Multidisciplinary Acute Care Research Organization (MACRO) is recruiting a Clinical Research Coordinator to work overnight shifts at multiple facilities in Pittsburgh. The CRC will maintain regulatory compliance, screen patients, monitor adverse events, coordinate study visits, and manage data entry with attention to source documentation.

Strong communication and computer skills are essential.

Qualifications

• Master's degree required or higher.
• At least 1 year of relevant experience in clinical research.
• Excellent communication and computer skills.

Responsibilities

• Maintain regulatory compliance.
• Screen patients for eligibility during overnight shifts.
• Monitor and report adverse events and unanticipated events.
• Coordinate protocol-related procedures and visits.
• Perform data entry and data management.
• Train staff on study protocols.

Skills

Communication skills

Independent work

Computer skills

Regulatory compliance

Education

Master's degree

Job description

The University of Pittsburgh's Multidisciplinary Acute Care Research Organization (MACRO) is recruiting a Clinical Research Coordinator to work overnight shifts at multiple facilities in Pittsburgh. The CRC will maintain regulatory compliance, screen patients, monitor adverse events, coordinate study visits, and manage data entry with attention to source documentation.

Strong communication and computer skills are essential.