UCSD Layoff from Career Appointment: Apply by 02/16/21 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor. Special Selection Applicants: Apply by 02/26/21. Eligible Special Selection clients should contact their Disability Counselor for assistance. DESCRIPTIONThe Assistant Clinical Research Coordinator coordinates the clinical and translational research efforts within the Division of Neonatology. Responsible for coordinating and managing clinical trials, including providing all aspects of protocol management such as screening for patient eligibility, data collection and analysis, sample collection and transport between institutions. ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files. Responsible for Human Research Protection Program (HRPP) formatting and submission of all relevant material, UCSD HRPP renewals and safety reports. Directly communicate with assigned physicians and nurses, attending regular Divisional research meetings. MINIMUM QUALIFICATIONSTheoretical knowledge of biology, microbiology, social sciences or related field, as typically attained by a Bachelor's degree and/or an equivalent combination of education and experience. Experience performing clinical research duties in a clinical research environment. Experience using statistical software applications. Knowledge of 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, experience in abstracting data from medical records. 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. 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. Thorough knowledge of x-rays, scans, and other diagnostic procedures. Experience completing clinical trials case report forms via hard copy and online. Excellent interpersonal, as well as written and verbal communication skills (using grammatically correct written English and accurate typing) to interact with a diverse population. Excellent phone etiquette skills. Demonstrated ability to interact effectively with diverse groups, including professional and non-professional staff and clients.
PREFERRED QUALIFICATIONS- Certification as a Clinical Research Associate or Coordinator.
- Experience working with research bulk accounts.
- Experience with investigational drug authorization criteria.
SPECIAL CONDITIONS- Employment is subject to a criminal background check and pre-employment physical.
- Must be willing/able to travel to different locations and work weekends and evenings as needed.
- Position may require travel between sites (Jacobs Medical Center, Rady Children's Hospital, and Rady Children's Hospital satellites).
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