Clinical Research Coordinator

Comrise; Salt Lake City (UT); On-site; USD 50,000 - 70,000; Full time

Job summary

A research organization in Salt Lake City is seeking a Research Coordinator responsible for coordinating multiple research protocols and acting as a liaison with local investigators and sponsors. The role requires a fundamental understanding of human subject research and adherence to research operations and regulations. Major responsibilities include data management, ensuring compliance with protocols, and attending study-related meetings. This is a critical position to support research integrity and patient safety.

Qualifications

• Understanding of research operations and regulations.
• Ability to coordinate multiple research protocols.
• Excellent communication skills for liaising between site and sponsors.

Responsibilities

• Coordinate multiple research protocols and serve as a liaison.
• Practice adherence to the Code of Conduct.
• Ensure timely and accurate data completion.

Job description

The Research Coordinator position is responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research.

Major Responsibilities

• Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”
• During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
• Performs routine operational activities for multiple research protocols
• Liaise between site research personnel, industry sponsors, and Supervisor
• Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
• Coordinates schedule of assessments from initial submission of feasibility until study closeout
• Reviews the study design and inclusion/exclusion criteria with physician and patient
• Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
• Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
• Creates study specific tools for source documentation when not provided by sponsor
• Collects, completes, and enters data into study specific case report forms or electronic data capture systems
• Generates and tracks drug shipments, device shipments, and supplies as needed
• Ensures timely and accurate data completion
• Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations
• Communicates all protocol-related issues to appropriate study personnel or manager
• Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required
• Reviews and responds to any monitoring and auditing findings.