Study Design Specialist (part-time)

Crio Inc.

4h

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, and conducting post-build quality control reviews. This individual will be considered an industry expert on the CRIO eSource module.

Requirements

• At least 1 year of healthcare experience.
• Ability to interpret clinical trial protocols, and source documents.
• Knowledge of medical terminology and procedures.
• 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 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.

Benefits

• Compensation Package - $20 an hour for all training and up to $450 for Study Design Build

What This Job Offers

• Job Type: Part-time
• Career Level: Entry Level