[Remote] Study Design Specialist
Note: The job is a remote job and is open to candidates in USA. CRIO is a health tech company focused on streamlining regulatory workflows in clinical research. The Study Design Specialist is responsible for creating comprehensive study builds in the CRIO platform, including developing eSource from protocols, conducting quality control reviews, and configuring budgets.
Responsibilities
- Utilize protocols, eCRF guidelines, pharmacy manuals, lab manuals, and other source documents to produce comprehensive builds for clients
- Interpret Clinical Trial Agreements and budgets for configuration in the CRIO finance module
- Design visit schedules and procedures for CTMS-only studies
- Complete client-requested edits and customizations
- Provide quality control reviews of client-built eSource and budget templates
- Manage complex trials to ensure all data is captured appropriately
- Modify standard templates to comply with protocol requirements
- Complete assignments on time
- Mentor and train current and new CRIO employees
Skills
- At least 1 year of healthcare experience
- Ability to interpret clinical trial protocols, source documents, and clinical trial agreements
- Knowledge of medical terminology and procedures
- Experience tracking study financials
- Strong people skills
- Detail-oriented with solid time management skills
- Well-organized, capable of establishing priorities, and executing tasks efficiently
- Experience with eSource, budget, and QC design in CRIO or other eSource/CTMS systems
- BS in medical or sciences field
- Experience as a Research Coordinator, Site Director, or Source Designer is a plus
Benefits
- Work from anywhere
- Unlimited PTO
- 401k company match
- Healthcare
- Dental
- Vision (Company Paid 100%)
- Life insurance
- Professional development
- Work From Home Expense Reimbursement
Company Overview
Company H1B Sponsorship