BACHELORS' DEGREE IN A SCIENTIFIC / TECHNICAL DISCIPLINE IS PREFERABLE
Responsibilities
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 pe r 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
Provide the UAT details to Validation Team and Study Data Manager
Completion of all activities as detailed in the relevant section of the developer checklist.
Forwards the Go Live / Training e-mail details to the Study Data Lead (SDL) for inclusion in the Go-Live e-mail
Review and promote SDS, Annotated eCRF, TandE, Blank eCRF..etc files in eTMF system
Confirms all required documents in eTMF system and Project Binder within Veeva
Location
Mumbai
Job Function
BUSINESS PROCESS SERVICES
Role
Executive
Job Id
383442
Desired Skills
Veeva vault
Desired Candidate Profile
Qualifications
: BACHELOR OF PHARMACY, BACHELOR OF SCIENCE (B.Sc), MASTER OF PHARMACY
Beware of fraud agents! do not pay money to get a job
MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.