Remote Study Design Specialist — eSource & Budget Expert

Crio, Inc; United States; Remote; USD 90,000 - 135,000; Full time

Benefits offered by this job

Unlimited PTO

401k match

Vision insurance

Life insurance

Professional development reimbursement

WFH expense reimbursement

Job summary

CRIO is seeking a Study Design Specialist to create comprehensive eSource builds from protocols, eCRFs, and budgets in the CRIO platform. You will conduct post-build QC reviews, configure budgets in the finance module, and mentor teammates.

The role emphasizes interpreting clinical trial agreements, budgets, and source documents, with a focus on data quality and trial efficiency. Remote work from anywhere in the US is supported.

Qualifications

• BS in medical or sciences field.
• Experience as Research Coordinator, Site Director, or Source Designer is a plus.
• At least 1 year of healthcare experience.
• Ability to interpret clinical trial protocols and source documents.
• Knowledge of medical terminology and procedures.
• Experience tracking study financials.
• Detail-oriented with solid time management skills.
• Well-organized with prioritization abilities.

Responsibilities

• Produce comprehensive builds from protocols and eCRFs in CRIO.
• Interpret budgets and configure in CRIO finance module.
• Design visit schedules for CTMS-only studies.
• Complete client-requested edits and customizations.
• Provide QC reviews of client-built eSource and templates.
• Manage complex trials to ensure data capture accuracy.
• Modify templates to meet protocol requirements.
• Complete assignments on time.
• Mentor and train CRIO staff.

Skills

eSource systems

Budget configuration

Quality control design

Protocol interpretation

CTMS familiarity

Mentoring

Time management

Detail orientation

Education

BS in medical or sciences

Tools

CRIO eSource

CRIO Finance module

Job description

CRIO is seeking a Study Design Specialist to create comprehensive eSource builds from protocols, eCRFs, and budgets in the CRIO platform. You will conduct post-build QC reviews, configure budgets in the finance module, and mentor teammates.

The role emphasizes interpreting clinical trial agreements, budgets, and source documents, with a focus on data quality and trial efficiency. Remote work from anywhere in the US is supported.