Data Coordinator
Data Coordinator
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
$ 55886 - 65000
1 Vacancy
Job Description
The purpose of this position is to independently coordinate and manage data entry for oncology treatment trials perform site initiation activities and facilitate the comprehensive compilation of research patient records according to federal regulations Good Clinical Practice and local and institutional policies. These responsibilities relate to the mission of the UNC / LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard institutional integrity.
Required Qualifications Competencies And Experience
Knowledge of ICH GCP Federal Regulations and Guidelines and ability to follow established regulations procedures and protocols. High level of accuracy and attention to detail. Strong computer skills. Ability to gather data and document procedures. Ability to plan work and coordinate multiple projects. Ability to contribute to preparation and delivery of reports trainings and SOPs. Customer oriented and ability to work in a team environment. Ability to communicate effectively and professionally verbally and in writing. Ability to work on evenings weekends and/or holidays occasionally required.
Preferred Qualifications Competencies And Experience
Previous experience with therapeutic clinical research involving drugs and/or devices. Experience in Phase I II and III clinical research. Experience navigating medical records and data extraction. Data Coordinator 1 is considered an entry level position. Data Coordinator 1 requires one year of data coordinator experience or experience in oncology clinical trials.
Work Schedule
Monday Friday 8:00AM 5:00PM
Required Experience:
Staff IC
Employment Type
Full-Time
