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.
- 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.
- 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. Apply today to embark on a rewarding career journey!
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
