Read and understand the protocol to be able to incorporate the data points into specification
Greater transparency with study team regarding timelines and impact of delays on overall
eCRF development timelines
With the Data Managers, attend and contribute to the study discussions.
Lead and Conduct eCRF Design Meetings
Document decisions and issues by creating backlog ID in Project Binder
during eCRF Design meetings
Develop eCRF screens as per the eCRF specification in Veeva Studio
Configure SDV/SDR, Safety and Coding within Veeva CDMS tool
To review the edit check specification document for clarity and to ensure checks are consistent and appropriate based on e-CRF design
Program new study specific checks, Protocol Deviation checks,
Email Checks as per edit check specifications (Should be aware of tips and best practices of Veeva Rules)
Validate and Perform developer level testing
Location
Mumbai
Job Function
BUSINESS PROCESS SERVICES
Role
Executive
Job Id
374054
Desired Skills
Life Sciences Domain
Desired Candidate Profile
Qualifications
: BACHELOR OF PHARMACY, BACHELOR OF SCIENCE ( B.Sc Degree ), MASTER OF PHARMACY, MASTER OF SCIENCE
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