Study Design Specialist (part-time)

Crio Inc.; United States; Remote; USD 28,000 - 41,000; Part time

Job summary

Crio Inc. seeks a Study Design Specialist to create study builds from protocols to eSource within the CRIO platform, including QC and post-build reviews. You will work with client documents to produce comprehensive eSource builds and mentor teammates.

Preferred candidates have experience with eSource/CTMS, a BS in medical or sciences, and strong time management and communication skills. This is a part-time role with training pay at $20/hour and up to $450 per study build.

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

• Create comprehensive study builds from protocols and source documents.
• Complete client-requested edits and customizations.
• Manage complex trials to ensure data capture.
• Modify templates to protocol requirements.
• Complete assignments on time.
• Mentor and train CRIO staff.

Skills

eSource design

Quality control

Time management

Mentoring

Communication

Education

BS in medical or sciences field

Tools

CRIO platform

eSource/CTMS systems

Job description

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.

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.

Preferred 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.

Other Qualifications:

• 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.

Join us at CRIO and be part of a dynamic team dedicated to revolutionizing the clinical research industry.

Equal Employment Opportunity

We’re proud to be an equal opportunity employer and welcome our employee’s differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status. Difference makes us better. Join us.

Benefits

This is a part time role:

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