Study Design Specialist

Crio Inc.

2d•$60,000 - $70,000•Remote

About The Position

The Study Design Specialist is responsible for creating comprehensive study builds from start to finish in the CRIO platform. This includes developing eSource from protocols and eCRFs, conducting post-build quality control reviews, and configuring budgets in our finance module. This individual will be considered an industry expert on the CRIO eSource and Finance modules.

Requirements

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.

Nice To Haves

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.

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.