Company: Thermo Fisher Scientific
Division: PPD Clinical Research Services
Location: Bangalore, Karnataka, India (Fully Remote)
Job Type: Full-Time
Shift: Second Shift (Afternoons)
Category: Clinical Research | Clinical Data Management (CDM) | EDC Programming
Experience Required: Minimum 4+ years in Clinical Data Management programming, including hands-on experience with Veeva Vault EDC
Role Overview
A leading global Contract Research Organization (CRO) is hiring a CDM Programmer II – Veeva Vault EDC to support database development and clinical data programming for international clinical trials. This fully remote opportunity is ideal for professionals with advanced expertise in Veeva Vault EDC, edit check programming, and regulatory-compliant data management processes.
The selected candidate will play a key role in designing, building, and validating clinical trial databases while ensuring adherence to Good Clinical Practice (GCP) and internal SOPs. This position requires technical proficiency, regulatory awareness, and strong cross-functional collaboration skills.
Key Responsibilities
Design, build, and test study databases and edit checks in Veeva Vault EDC.
Manage retrospective amendments and database updates in accordance with study requirements.
Define and import clinical data into EDC systems.
Create, test, and validate listings for data review and query management.
Perform programming activities aligned with project specifications and timelines.
Lead simple to moderately complex studies under supervision.
Identify and resolve technical issues related to database programming and system configuration.
Contribute to process optimization initiatives to improve operational efficiency.
Ensure compliance with ICH-GCP guidelines and departmental SOPs.
Support development of internal training materials and knowledge-sharing initiatives.
Education & Experience
Bachelor’s degree in Life Sciences, Computer Science, Biotechnology, Biostatistics, or a related discipline.
Minimum 4+ years of experience in clinical data programming within pharmaceutical, biotechnology, or CRO environments.
Proven hands-on expertise in Veeva Vault EDC database build and edit check programming.
Equivalent combinations of education and directly related experience may be considered.
Technical Skills & Competencies
Strong working knowledge of Veeva Vault EDC.
Experience with SAS, SQL, Medidata Rave, and related programming tools.
Solid understanding of relational database systems (RDBMS).
Knowledge of clinical trial workflows and regulatory data standards.
Familiarity with retrospective amendment management.
Strong analytical and troubleshooting skills.
Excellent organizational skills with the ability to manage multiple priorities and tight timelines.
Demonstrated ability to work in cross-functional, multi-disciplinary project teams.
Strong project management awareness including timelines, risk management, and budget considerations.
Delivery-focused with high attention to data quality and compliance.
Work Environment
Fully Remote (India-based role)
Second Shift (Afternoon schedule)
Office-based virtual environment
Occasional domestic or international travel may be required based on project needs
About the Organization
Thermo Fisher Scientific is a global leader in serving science, supporting pharmaceutical and biotechnology organizations worldwide. Through its clinical research division PPD, the company has contributed to thousands of clinical trials across more than 100 countries, partnering with leading pharmaceutical companies and emerging biotech innovators.
The organization is known for scientific excellence, regulatory expertise, and technology-driven clinical development solutions that accelerate drug development and improve patient outcomes globally.
Equal Opportunity & Accessibility
The organization provides reasonable accommodations for individuals with disabilities throughout the hiring and employment process.
As an Equal Opportunity Employer, all qualified applicants will receive consideration without discrimination based on legally protected characteristics.
Apply via ThePharmaDaily.com
If you are an experienced Clinical Data Management professional with strong Veeva Vault EDC expertise seeking a remote CRO opportunity, apply now through ThePharmaDaily.com and advance your career in global clinical trial data programming and regulatory-compliant data management.
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