UCSD Layoff from Career Appointment: Apply by 9/13/17 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor. Eligible Disability Counseling and Consulting services (DCC) or Special Selection clients should contact their Vocational Rehabilitation Counselor for assistance.
The Clinical Research Manager independently oversees and manages research protocols for the Division of Neonatology. Coordinate and oversee research start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of subjects. Create informational and recruitment materials and act as a liaison with other UCSD departments and community clinics / agencies for the purpose of implementation of studies. The Clinical Research Manager will plan, develop and implement start-up procedures for multiple research studies as well as lead, direct, and coordinate operational efforts. Assure compliance with state and federal regulatory guidelines. Oversee the quality of the medical and clinical research data. Provide direction to Clinical Trials Office and guidance to investigators. Provide education and information to the general public concerning the ongoing clinical trials. Independently create original documents and policies for the Division. Work closely with federal and state regulatory officials. Participate in the preparation and negotiations for Clinical Trials budgets and prepare, analyze, and manage the Division's research budgets.
Theoretical knowledge in a social science or basic science such as Biology, Microbiology or a related field.
Possess a Clinical Research Coordinator Certificate, or Master's Degree.
Ability to discern items that can be handled independently and those which require attention of supervisor, including ability to quickly determine subject matter of material and necessary action to be taken in a timely manner.
Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.
Working knowledge of medical and scientific terminology.
Computer proficiency, including working knowledge of word processing, spreadsheet software (Microsoft Office) and internet browser applications. Experience in conducting searches on the internet.
Strong experience in clinical trials research.
Advanced knowledge of experimental protocols, data gathering, protocol design and evaluation.
Must have access to transportation, work occasional overtime, and travel to various clinic sites approximately 5% of the time to oversee research studies.
Must successfully complete pre-employment physical and annual TB screen.
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