Back
Tier-1 brand, metro location, and mid-level title increase competition; niche EDC/Veeva skills moderate density.
Requires clinical trials, GxP/ICH knowledge and Veeva EDC skills, limiting cross-industry transferability.
Regulatory (GxP/ICH), Veeva/EDC, and clinical study experience requirements increase shortlisting strictness.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Lead technical development and study set-up activities for Electronic Data Capture (EDC) solutions across one or more clinical studies.
Manage technical and vendor oversight for multiple data types and ensure delivery of study eDC applications with quality and timeliness.
Drive process improvements, quality control, and risk communication to Study Data Manager, supporting clinical study delivery and compliance with regulatory standards.
Experience Required: Work Experience Required: Not explicitly mentioned in the JD
Proficiency in Electronic Data Capture (EDC) systems and programming languages such as Python.
Strong knowledge of GxP, ICH requirements, and external regulations governing drug development.
Ability to oversee multiple vendors and manage study specification documents including operational requirements and translations.
Experienced in clinical study data acquisition with operational responsibility for EDC study setup and vendor management.
Demonstrates expertise in applying regulatory standards (GxP, ICH) to data acquisition processes in a drug development context.
Capable of coordinating technical development and quality assurance for complex clinical studies with multiple data types and stakeholders.