Clinical Research Coordinator, Integrated Research, Per Diem, Day Shift

Adventist Health•Glendale, CA

11d

About The Position

Nestled between Burbank and Pasadena, Adventist Health Glendale is one of the area's leading healthcare providers. We are comprised of a 515-bed hospital, two urgent cares, home care services, comprehensive cardiology care and a vast scope of services located in the San Fernando Valley. We are committed to the development and empowerment of our nurses and have received Magnet designation from the American Nurses Credentialing Center. Glendale is known for its urban living, with easy access to dining, entertainment, shopping, amusement parks and outdoor recreation. Adventist Health Glendale is proud to be part of the thriving, diverse community since 1905. Job Summary: Coordinates and participate in clinical research studies conducted by principal investigator(s). Coordinates and participate in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Coordinates and performs study specific regulatory processes across multiple studies of different therapeutic areas and phases, in accordance to appropriate regulations, Standard Operating Procedures (SOPs), and study specific protocols/plans and processes. Applies substantial knowledge and experience to perform a wide range of advanced activities and/or determines how to use resources to meet schedules and goals; serves as working supervisor for team or work group. Coordinates small program(s) with limited budget/impact.

Requirements

Bachelor’s Degree or equivalent (some certifications will require Bachelor’s): Required

Nice To Haves

Master's Degree
Clinical Research Coordinator Certification

Responsibilities

Coordinates and implements procedures to collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.
Codes, evaluates and interprets collected data and prepares appropriate documentation.
Obtains blood samples, cultures, tissues and other specimens for laboratory analysis.
Ensures compliance with protocol guidelines and requirements of regulatory agencies.
Identifies problems and/or inconsistencies and monitors patients' progress to include documentation and reporting of adverse events.
Recommends corrective action as appropriate.
Evaluates and interprets collected clinical data in conjunction with principal investigator(s) as appropriate.
Prepares oral presentations or written reports and analyses setting forth progress, trends and appropriate recommendations or conclusions.
Assures compliance of general and study specific regulatory related processes and applicable regulations for the reporting of events to regulatory agencies.
Develops appropriate regulatory reports and associated documentation in accordance with standard of practices and study specific processes, and maintains primary responsibility of a variety of regulatory tasks including: assess, complete, and submit protocol related documents to the appropriate committees.
Performs other job-related duties as assigned.