Clinical Data Manager, Flexible Hybrid
Los Angeles, California
Employer: UCLA Health
Industry: Ambulatory/Clinical Care Services
Salary: Competitive
Job type: Full-Time
Description
The Clinical Data Manager will be responsible for data management of clinical research studies. You will collect and transcribe research patient data and study related information into research records and maintain study patient files. You will work with study monitors to collect accurate data in a timely manner and assist investigators and study coordinators in clinic settings.
You may also be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner, under the supervision of the Principal Investigator. Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. You will ensure investigational product is adequately managed and documented.
Work may be assigned by the manager, team leader, investigator or Senior Management, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. The ideal candidate would be available occasionally to work flexible hours to meet study or CRU deadlines and priorities.
Hourly Salary Range: $32.65 - $52.53
The Clinical Data Manager will be responsible for data management of clinical research studies. You will collect and transcribe research patient data and study related information into research records and maintain study patient files. You will work with study monitors to collect accurate data in a timely manner and assist investigators and study coordinators in clinic settings.
You may also be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner, under the supervision of the Principal Investigator. Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. You will ensure investigational product is adequately managed and documented.
Work may be assigned by the manager, team leader, investigator or Senior Management, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. The ideal candidate would be available occasionally to work flexible hours to meet study or CRU deadlines and priorities.
Hourly Salary Range: $32.65 - $52.53
Created: 2024-06-18
Reference: 19062747
Country: United States
State: California
City: Los Angeles
ZIP: 90291
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