Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Duties include:
Work with the Internal Review Board with submissions and approvals
Maintain the sponsor provided regulatory files and ensure all documents are saved in the appropriate files (electronic/paper)
Quality inspection of Source Documents
Assist with Electronic Data Capture and Source documents
Assist with maintaining and updating SOP's for research department
Filing crucial and private documents per the Sponsor's specifications
Maintaining and updating staff documents (CV's, licenses, etc.)
Communication with staff members regarding completing trainings, staff meetings and updating information as received by sponsors, lab vendors and CRAs.
Working with staff to communicate with subjects (email, phone and first class mail)
Answering phones on a multi-line phone system
Assist with scheduling patient and sponsor visits
Various other clerical duties as needed
High School Diploma
Good communication skills
Proficient in Microsoft Word, Excel and Outlook
Knowledge of Medent (preferred)
Associate degree in business, Medical and or Finance (preferred).
Job Type: Full-time
Pay: From $16.00 per hour
Benefits:
Schedule:
Education:
Ability to Relocate:
Work Location: In person
0 Clinical Research Coordinator jobs found in Clay, NY area