Clinical DB Designer
IQVIA
full-time
Posted on:
Location Type: Office
Location: Kochi • 🇮🇳 India
Visit company websiteJob Level
JuniorMid-Level
About the role
- Interprets the study protocol.
- Design and update the eCRF.
- Create and update Edit Specification Document.
- Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)
- Complete the Study Authorization Form and Trial Capacity Request Form (InForm)
- Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting.
- Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.
- Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.
- Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.
- Escalate potential quality issues.
- Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.
- Reviews build timelines and provide input as applicable.
Requirements
- Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req
- 0-2 years of relevant core Technical designer experience and total exp being 5+ yrs. Req
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
eCRF designEdit Specification DocumentEDC build componentsdatabase designLLRR data collectionproject risk communicationproject-specific training documentationStandard Operating Procedures
Soft skills
facilitationcommunicationleadershipdiscussion leadership