Study Design Specialist

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.
• Create 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.

Qualifications

• 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.
• 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.