Study Design Specialist
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Job Description
Study Design Specialist crafting comprehensive study builds for clinical research using the CRIO platform. Requires expertise in eSource, budgets, and quality control in healthcare.
Responsibilities:
- Utilize protocols, eCRF guidelines, pharmacy manuals, lab manuals, and other source documents to produce comprehensive builds for clients.
- Interpret Clinical Trial Agreements and budgets for configuration in the CRIO finance module.
- Design visit schedules and procedures for CTMS-only studies.
- Complete client-requested edits and customizations.
- Provide quality control reviews of client-built eSource and budget templates.
- 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.
Requirements:
- Experience with eSource, budget, 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, source documents, and clinical trial agreements
- Knowledge of medical terminology and procedures
- Experience tracking study financials
- Strong people skills
- Detail-oriented with solid time management skills
- Well-organized, capable of establishing priorities, and executing tasks efficiently
Benefits:
- Work from anywhere
- Unlimited PTO
- 401k company match
- Healthcare
- Dental
- Vision (Company Paid 100%)
- Life insurance
- Professional development
- Work From Home Expense Reimbursement
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