Clinical Research Project Manager - Sylmar, United States - OLIVE VIEW-UCLA EDUCATION AND RES INSTITUTE

Description

We are looking for a Full Time Clinical Research Project Manager to manage our research team in the Department of Emergency Medicine Research Division at Olive View-UCLA Medical Center.

Our team's research focuses on the intersection of emergency medicine and infectious diseases affecting the community. Current activities include surveillance of mpox, observational study of antibiotic resistant bacteria in skin infections, and a clinical trial to determine best duration of antibiotic treatment for women with kidney infections,


RESPONSIBILITIES

• Manage all active studies for OV-UCLA DEM research team under the PI's and research director's supervision
• Recruit, hire and manage schedules and activities of OV-UCLA study coordinator staff
• Manage the set up, implementation/data collection, data quality assurance, regulatory activities, and close out of all studies
• Work with micro lab staff and research pharmacists as necessary to set up and implement specimen collection, testing, storage and study drug dispensing procedures for relevant studies
• Ensure participant and staff compensation are set up, accounted for and tracked during study implementation
• Train and retrain study coordinator staff as necessary
• Schedule and run regular meetings with OV-UCLA study coordinator staff and PIs as necessary.

JOB QUALIFICATIONS

• Excellent verbal and written communication skills, which may include business and technical writing, editing and proofreading.
• Computer skills using PC platform computers with proficiency in Excel, Word, Access, Powerpoint.
• Demonstrated organizational skills to efficiently and effectively provide management/monitoring support for multiple clinical studies and projects, providing accurate information in a timely manner.
• Demonstrated understanding of confidential information, how it is defined, and demonstrated skill in maintaining confidential status of such information.
• Demonstrated ability to prioritize workload to meet demands of above PI's and supervisor.
• Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data collection, etc.
• Demonstrated interpersonal skills to work with patients, their families/ guardians, physicians, administrators, work colleagues, representatives from sponsors and other to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.

Job Types:
Full-time, Part-time


Pay:
$ $50.00 per hour

Expected hours: 40 per week


Benefits:

• 401(k)
• 401(k)

matching

• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance

Schedule:

• Monday to Friday

Work Location:
In person