Responsibilities:
- Development of eCRF to meet the needs of the customer and the clinical trial utilizing protocol and specifications provided at the pre-design meeting. Understand Quintiles EDC processes and the requirements on the design for reporting and study management.
- Advise and provide justification for design decisions to Technical Lead and at Design Meeting.
- Responsible for optimal design reducing the number of edit checks required, ensuring good system performance, and the utilization of global/client specific libraries to ensure consistency and efficiency.
- This role will eventually (3-6 months after starting) be responsible for providing a draft Edit Check Specification to the DTL.
- Requires good communication skills and this role will work closely with the Study DTL and Technical Lead and Validation Team Lead
- Requires a technically logical thinker to resolve questions and issues with the Technical Lead, DTL and VTL. This role will need to have a good knowledge of forms design, data flow, and the impact of design on the system.
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