Clinical Research Coordinator - Medicine - 140230

About the role

The MASLD Research Center focuses on the etiology, contributing factors, natural history, complications, and therapy of Metabolic dysfunction-associated steatohepatitis (MASH) and metabolic dysfunction-associated steatotic liver disease (MASLD). The Clinical Research Coordinator will coordinate and oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of subjects.

Responsibilities

• Coordinate and oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of subjects for multiple phase I-III research studies.
• Create informational and recruitment materials and act as a liaison with other UCSD departments and agencies for the purpose of implementation of studies.
• Plan, develop, and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct, and help to coordinate operational efforts.
• Affirm compliance with state and federal regulatory guidelines, oversee the quality of the medical and clinical research data, provide direction and guidance to investigators, and provide education and information to the general public concerning the ongoing clinical trials.
• Assist Principal Investigators (PIs) with proposals, progress reports, and manuscripts, independently create original documents and policies for assigned disease teams, and work closely with federal and state regulatory officials when/if indicated.
• Provide training, data and chart management, quality assurance checks for studies, provide backup to research center activities, and work closely with the Clinical Research Supervisor.

Requirements

• Strong theoretical knowledge as typically attained by a Bachelor's Degree in a social science or basic science such as Biology, Microbiology or a related field and/or an equivalent combination of education and work experience.
• Demonstrated experience in clinical trials research.
• Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
• Strong experience in clinical trials research including budget negotiations and invoicing per clinical trial agreement.
• Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
• Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.
• Knowledge of cost accounting as applied to both University and Medical Center functions.
• Knowledge of medical billing and collections guidelines and procedures.

Qualifications

• Bachelor's Degree in a social science or basic science such as Biology, Microbiology or a related field.
• Equivalent combination of education and work experience.
• Demonstrated experience in clinical trials research.

Skills

• Strong theoretical knowledge as typically attained by a Bachelor's Degree in a social science or basic science such as Biology, Microbiology or a related field and/or an equivalent combination of education and work experience.
• Demonstrated experience in clinical trials research.
• Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
• Strong experience in clinical trials research including budget negotiations and invoicing per clinical trial agreement.
• Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
• Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.
• Knowledge of cost accounting as applied to both University and Medical Center functions.
• Knowledge of medical billing and collections guidelines and procedures.

Benefits

N/A

Pay

$38.74 - $62.29 / Hour

Schedule

Days, 8-Hour Shifts, Monday-Friday