eSource Study Design Specialist (Part-Time)

CRIO; United States; On-site; USD 28,000 - 41,000; Part time

Job summary

CRIO is seeking a Study Design Specialist to build comprehensive eSource from protocols and eCRFs, and perform post-build QC reviews within the CRIO platform. This role requires attention to detail and the ability to mentor teammates while ensuring accurate data capture across complex trials.

The candidate will adapt templates to protocol requirements, manage multiple studies, and collaborate with cross-functional teams to deliver high-quality, on-time results.

Qualifications

• Experience with eSource 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.
• Complete client-requested edits and customizations.
• 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

eSource and QC design experience

Research coordination

Detail-oriented

Education

BS in medical or sciences field

Job description

CRIO is seeking a Study Design Specialist to build comprehensive eSource from protocols and eCRFs, and perform post-build QC reviews within the CRIO platform. This role requires attention to detail and the ability to mentor teammates while ensuring accurate data capture across complex trials.

The candidate will adapt templates to protocol requirements, manage multiple studies, and collaborate with cross-functional teams to deliver high-quality, on-time results.