UC San Diego Health
Lead Research Program Coordinator - 136642
UC San Diego Health, San Diego, California, United States, 92189
Lead Research Program Coordinator - 136642
Join the Department of Pediatrics at UC San Diego Health as a Lead Research Program Coordinator. The Department of Pediatrics is one of the largest departments within the School of Medicine, with a consolidated budget of approximately $106 million. The department has undergone significant growth in recent years and is expected to continue expanding its research and clinical portfolio. Under the general direction of the Research Program Manager, the Lead Research Program Coordinator acts as a fully operational Clinical Research Coordinator, leading a team of Assistant Clinical Research Coordinators and assisting with managing multi-site prospective pregnancy registry studies. Responsibilities include protocol management, patient recruitment and follow-up, data collection, ensuring protocol compliance, and maintenance of accurate and complete clinical research files. The incumbent will also provide training to interview staff and students, delegate workload, and generate reports. Minimum Qualifications: Four years of related experience, education/training, or theoretical knowledge of biology, microbiology, social sciences, clinical sciences as typically attained by a Bachelor's degree. Experience performing clinical research duties in a clinical research environment. Experience using database, word processing, and spreadsheet applications such as Velos, Access, Excel, and MS Word. Experience with laboratory procedures and values and experience in interpreting them to determine patient eligibility and potential toxicities. Experience working with FDA policies regulating clinical trials. Experience in medical assessment and patient interviewing to determine toxicities related to protocol management. Experience interpreting medical charts and abstracting data from medical records. Experience with clinical trials participant or study subject recruitment. Experience coordinating study startup activities. Experience providing in-service training to various research personnel on protocols, processes, and procedures. Knowledge of x-rays, scans, and other diagnostic procedures. Experience maintaining files and keeping records. Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting. Excellent interpersonal, written, and verbal communication skills. Ability to work independently and maintain confidentiality. Preferred Qualifications: Certification as a Clinical Research Associate or Coordinator. Experience working with research bulk accounts. Experience with investigational drug authorization criteria. Experience providing delegation, training, and leadership to staff. Knowledge of National Institute of Health (NIH), Good Clinical Practice (GCP), Injury and Illness Prevention Program (IIPP), Human Resource Protection Program (HRPP), IATA Shipping of Blood Specimens, and Bloodborne Pathogens. Completion of courses or certification in leadership. The University of California is committed to fostering a rich and diverse environment, inclusive and supportive of all students, faculty, staff, and visitors.
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Join the Department of Pediatrics at UC San Diego Health as a Lead Research Program Coordinator. The Department of Pediatrics is one of the largest departments within the School of Medicine, with a consolidated budget of approximately $106 million. The department has undergone significant growth in recent years and is expected to continue expanding its research and clinical portfolio. Under the general direction of the Research Program Manager, the Lead Research Program Coordinator acts as a fully operational Clinical Research Coordinator, leading a team of Assistant Clinical Research Coordinators and assisting with managing multi-site prospective pregnancy registry studies. Responsibilities include protocol management, patient recruitment and follow-up, data collection, ensuring protocol compliance, and maintenance of accurate and complete clinical research files. The incumbent will also provide training to interview staff and students, delegate workload, and generate reports. Minimum Qualifications: Four years of related experience, education/training, or theoretical knowledge of biology, microbiology, social sciences, clinical sciences as typically attained by a Bachelor's degree. Experience performing clinical research duties in a clinical research environment. Experience using database, word processing, and spreadsheet applications such as Velos, Access, Excel, and MS Word. Experience with laboratory procedures and values and experience in interpreting them to determine patient eligibility and potential toxicities. Experience working with FDA policies regulating clinical trials. Experience in medical assessment and patient interviewing to determine toxicities related to protocol management. Experience interpreting medical charts and abstracting data from medical records. Experience with clinical trials participant or study subject recruitment. Experience coordinating study startup activities. Experience providing in-service training to various research personnel on protocols, processes, and procedures. Knowledge of x-rays, scans, and other diagnostic procedures. Experience maintaining files and keeping records. Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting. Excellent interpersonal, written, and verbal communication skills. Ability to work independently and maintain confidentiality. Preferred Qualifications: Certification as a Clinical Research Associate or Coordinator. Experience working with research bulk accounts. Experience with investigational drug authorization criteria. Experience providing delegation, training, and leadership to staff. Knowledge of National Institute of Health (NIH), Good Clinical Practice (GCP), Injury and Illness Prevention Program (IIPP), Human Resource Protection Program (HRPP), IATA Shipping of Blood Specimens, and Bloodborne Pathogens. Completion of courses or certification in leadership. The University of California is committed to fostering a rich and diverse environment, inclusive and supportive of all students, faculty, staff, and visitors.
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