CDM Programmer II (Veeva Vault EDC) – Clinical Data Management
Location: Bangalore, Karnataka, India
Job ID: R-01340606
Job Type: Full-Time
Category: Clinical Research
Work Mode: Fully Remote
Work Schedule: Second Shift (Afternoons)
Work Environment: Office-Based
Job Overview
A leading global clinical research organization under Thermo Fisher Scientific is seeking an experienced CDM Programmer II with expertise in Veeva Vault EDC to support clinical data management operations and programming deliverables. This role focuses on database development, data validation, and process optimization to ensure accuracy, compliance, and efficiency in clinical trial data management.
The selected candidate will collaborate with multidisciplinary project teams to manage clinical data systems, improve data workflows, and contribute to high-quality clinical research outcomes across global trials.
Key Responsibilities
Perform assigned programming and data management tasks within defined project timelines and departmental procedures.
Design, build, and test clinical project databases and edit checks using Veeva Vault EDC.
Manage retrospective amendment processes and ensure data consistency across studies.
Define, import, and validate clinical data within data management systems.
Create and test data listings for review and perform programming activities aligned with project requirements.
Lead studies of simple to moderate complexity under supervision and resolve technical challenges effectively.
Participate in process improvement initiatives to enhance operational efficiency.
Ensure adherence to departmental standard operating procedures (SOPs) and working practice guidelines.
Contribute to the development of training materials and procedural documentation.
Support cross-functional teams in achieving project deliverables within scope and budget.
Technical Skills and Competencies
Strong experience in Veeva Vault EDC database design and configuration.
Working knowledge of programming and data management tools such as SAS, SQL, Rave, and Veeva Vault.
Understanding of retrospective amendment management in clinical trials.
Strong knowledge of clinical data management processes and regulatory requirements.
Excellent written, verbal, and technical communication skills.
Strong analytical thinking and problem-solving abilities.
Ability to manage multiple priorities and work under tight deadlines.
Knowledge of Good Clinical Practice (GCP) guidelines and applicable standard operating procedures.
Demonstrated ability to identify and resolve technical issues in professional environments.
Strong leadership capabilities and ability to collaborate with multidisciplinary project teams.
Project management skills, including budget management and risk mitigation.
Quality-focused and delivery-driven approach.
Educational Qualifications and Experience Required
Bachelor’s degree or equivalent academic or vocational qualification in life sciences, computer science, or a related field.
Minimum 4+ years of relevant experience in clinical data management, database programming, or clinical research systems, particularly Veeva Vault EDC.
Equivalent combinations of education, training, and directly related experience may be considered.
Working Conditions
Work performed in an office-based environment with standard office equipment.
Occasional travel to project sites, including domestic and international travel, may be required based on business needs.
Uttar Pradesh :
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