Study Design Specialist – Part-Time

This is a fully remote position, open to applicants in United States.

📋 Description

• Develop thorough study builds from inception to completion using the CRIO platform.

• Create eSource based on protocols and electronic Case Report Forms (eCRFs).

• Perform quality control reviews after the build process.

• Leverage protocols, eCRF guidelines, pharmacy manuals, lab manuals, and other source materials to deliver detailed client builds.

• Execute edits and customizations as requested by clients.

• Oversee complex trials to ensure accurate data collection.

• Adjust standard templates to meet specific protocol requirements.

• Complete tasks within established timelines.

• Provide mentorship and training to both current and new CRIO staff.

⛳️ Requirements

• Prior experience with eSource and quality control design in CRIO or similar eSource/CTMS systems is preferred.

• Bachelor’s degree in a medical or scientific discipline is preferred.

• Experience as a Research Coordinator, Site Director, or Source Designer is a plus.

• Minimum of 1 year of experience in the healthcare field.

• Capability to interpret clinical trial protocols and source documentation.

• Familiarity with medical terminology and procedures.

• Excellent interpersonal skills.

• Attention to detail with strong time management capabilities.

• Highly organized, able to set priorities, and execute tasks effectively.

🏝️ Benefits

• Up to $450 for Study Design Build.

• Flexible part-time schedule.

• Opportunity for remote work.