FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Veeva EDC programming and eCRF design, with a strong understanding of clinical data standards and governance processes. Capable of optimizing library components for reusability while ensuring compliance with protocol requirements and integration with clinical systems.
Highest-signal resume keywords
Veeva EDC ProgrammingECRF DesignClinical Data StandardsLibrary DevelopmentStakeholder Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
ECRF SpecificationsEdit-Check SpecificationsDynamicsDerivationsUAT Scripts DevelopmentDatabase TroubleshootingSDTM StructuresCQLCDBJSON
Soft Skills
Problem-SolvingCross-Functional CollaborationIndependent ContributorStakeholder ManagementAbility to Recommend Improvements
Tools & Technologies
Veeva EDCCTMSSASRPythonData WarehousesSharePoint
Industry Keywords
Clinical ResearchData ManagementGovernance ProcessesInspection ReadinessTMF Documentation
Tech Stack
Tools & technologiesPython
About the role
Key responsibilities & impact- Design, develop, validate, and maintain reusable eCRFs and library components within Veeva EDC
- Create and maintain eCRF specifications, edit-check specifications, dynamics, and derivations
- Establish library collections, version control, change management, and governance processes
- Ensure library components align with clinical data standards and protocol requirements
- Optimize library design to balance reusability, study needs, and ongoing maintenance
- Support lab modules and integrations with IRT, safety, coding, local laboratories, and other clinical systems
- Develop and execute UAT scripts and validate EDC configurations
- Understand how library components are consumed and implemented at the study level
- Troubleshoot database and library-configuration issues and implement post-production changes
- Understand backend EDC data, raw/CDM outputs, SDTM structures, and downstream data-model requirements
- Partner with Data Management, Standards, Clinical Operations, Clinical Supplies, IT, Quality, CROs, and technology vendors
- Support EDC standards, governance models, inspection readiness, and TMF documentation
- Identify opportunities to automate and streamline the specification-to-build process
- Track deliverables, milestones, risks, and quality metrics
Requirements
What you’ll need- Bachelor’s degree or equivalent relevant experience
- 6+ years of experience in Data Management, EDC programming, Clinical IT, or related clinical-research functions
- 3–5 years of hands-on Veeva Library development and maintenance experience
- Strong hands-on experience with Veeva EDC is mandatory
- Experience in eCRF design, EDC programming, edit checks, dynamics, derivations, and lab modules
- Knowledge of clinical data standards and protocol interpretation
- Experience with reusable components, library collections, version control, and governance
- Understanding of blinded and unblinded study configurations
- Experience integrating EDC with laboratories, safety systems, IRT, coding, and other clinical-trial modules
- Understanding of raw/CDASH, SDTM structures, and downstream data consumption
- Experience with CQL, CDB, JSON, or C# is preferred but not mandatory
- Understanding of CTMS, SAS, R, Python, data warehouses, or SharePoint is advantageous
- Independent lead contributor who can translate broad requirements into workable solutions
- Ability to think beyond provided specifications, challenge assumptions, and recommend improvements
- Strong problem-solving, stakeholder-management, and cross-functional collaboration skills
- Ability to deliver confidently with limited supervision and reduced review cycles
- Legal right to work in the country where the role is based
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways