Builds and maintains clinical research projects in clinical research management systems. Creates visit and procedure calendars and enters budget and payment information.
Essential Functions:- Supports technical needs of end users in a timely manner by creating Study Protocols in clinical research management system, including related Calendars, Procedures, Visits, Forms, Budgets, etc.
- Demonstrates a working knowledge of the components of a clinical research protocol; can identify procedural components to be budgeted.
- Collaborates with Feasibility Coordinators and study teams regarding data requirements and accuracy for studies of varying complexity
- Participates in data migration-related activities and data entry related to study protocol requirements.
- Works with Feasibility Coordinator and/or Clinical Research Business Operations Team Lead to ensure issues are resolved in a timely manner.
- Ensures accuracy of calendars, budgets and payment information to ensure compliance with billing regulations and to meet organizational reporting needs.
- Ensures accuracy and completeness of payment terms to maximize revenue capture.
- Assists builds in other clinical research management systems i.e., eRegulatory, eConsent, RedCap, Smartsheets etc.
Education Requirement:Bachelor’s Degree or equivalent experience, required.
Licensure Requirement:(not specified)
Certifications:(not specified)
Skills:- Accountability in task ownership and solution-oriented work approach.
- Ability to work independently using initiative and good judgment.
- Working knowledge in the use of information technology.
- Strong organizational skills including attention to detail and multi-tasking.
- Ability to filter information, discern importance and efficiently execute tasks.
- Excellent verbal and written communication skills.
Experience:- Experience in an applied data management or services role, required.
- On