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Study Design Specialist - Part Time

Posted 2024-11-07

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💎 Seniority level: Junior, At least 1 year

📍 Location: United States

💸 Salary: 20 - 450 USD per hour

🔍 Industry: Health tech

🏢 Company: Clinical Research IO (CRIO)

⏳ Experience: At least 1 year

🪄 Skills: Organizational skills

Requirements:
  • Experience with eSource and QC design in CRIO or other eSource/CTMS systems.
  • BS in medical or sciences field is preferred.
  • 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.
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.
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