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Role at a glance
You will
Interpret study protocols and design electronic Case Report Forms (eCRFs)
Create and update Edit Specification Documents and generate specifications for Electronic Data Capture (EDC) build components
Complete study authorization forms and trial capacity request forms
Experience
0–2 years
Job description
Location: Kochi, India Department: Data Science
We are seeking a Clinical Database Designer to join our team in Kochi, India. As a Clinical Database Designer, you will be responsible for study design, editing specifications, and system configurations. You will work closely with other project stakeholders to ensure the timely delivery of high-quality study design components.
Key Responsibilities:
Interpret study protocols and design electronic Case Report Forms (eCRFs)
Create and update Edit Specification Documents and generate specifications for Electronic Data Capture (EDC) build components
Complete study authorization forms and trial capacity request forms
Attend meetings, including Pre-Design Meetings, Online Screen Review Meetings, and Internal Design Review Meetings
Facilitate internal Edit Specification Review Meetings and lead discussions on Edit Specification Documents
Design databases to collect data and ensure proper access controls
Communicate project risks and escalate potential quality issues
Stay up-to-date with required Standard Operating Procedures and complete project-specific training
Requirements:
Bachelor's degree in Science, Computer Science, Information Technology, or Technology
0-2 years of relevant technical designer experience and 5+ years of total experience
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Questions you may be asked
Tell me about yourself.
Explain the four pillars of object-oriented programming.
What is the difference between a process and a thread?
