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Cdm Programmer -Ii ( Veeva Vault Edc )

Thermo Fisher Scientific
Thermo Fisher Scientific
4+ years
preferred by company
10 Feb. 10, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

CDM Programmer II – Veeva Vault EDC

Location: Bangalore, Karnataka, India
Job ID: R-01340606
Employment Type: Full-Time
Work Mode: Fully Remote
Work Schedule: Second Shift (Afternoon)
Category: Clinical Research / Clinical Data Management


About the Organization

Thermo Fisher Scientific, through its PPD® clinical research portfolio, is a leading global contract research organization (CRO) supporting pharmaceutical and biotechnology companies in delivering innovative therapies worldwide. With operations spanning over 100 countries and thousands of clinical trials, the organization brings deep scientific, technical, and operational expertise to accelerate drug development and improve global health outcomes.


Job Overview

The CDM Programmer II – Veeva Vault EDC will provide advanced clinical data programming and system support for global clinical trials. This role focuses on Veeva Vault EDC database build, edit check development, data validation, and retrospective amendment management, ensuring high-quality, compliant data delivery. The position is ideal for experienced clinical data professionals who thrive in remote, fast-paced, and cross-functional environments.


Key Responsibilities

Clinical Data Programming & EDC Management

  • Design, build, and test clinical trial databases and edit checks using Veeva Vault EDC

  • Manage retrospective amendments, including impact assessment, implementation, and validation

  • Define, import, and validate clinical data in alignment with study protocols and data standards

  • Develop, test, and maintain listings for clinical data review

Study Support & Execution

  • Execute programming tasks in accordance with project timelines, contractual obligations, and departmental SOPs

  • Act as lead programmer on studies of simple to moderate complexity under appropriate supervision

  • Research and apply new programming techniques and tools to resolve technical challenges

Quality, Compliance & Process Improvement

  • Ensure compliance with GCP, SOPs, and regulatory requirements

  • Participate in process improvement initiatives to enhance efficiency and data quality

  • Contribute to the development of informal training materials and knowledge-sharing activities

  • Maintain accurate documentation of programming activities and system configurations


Education & Experience Requirements

Educational Qualifications

  • Bachelor’s degree or equivalent in Life Sciences, Computer Science, Information Technology, or a related field

Professional Experience

  • Minimum 4+ years of relevant experience in clinical data management or clinical data programming

  • Hands-on experience with Veeva Vault EDC database build and study maintenance

  • Equivalent combinations of education, training, and directly related experience may be considered


Required Skills & Competencies

Technical Skills

  • Strong working knowledge of Veeva Vault EDC

  • Experience with SAS, SQL, and Oracle Clinical / Medidata Rave or similar EDC platforms

  • Understanding of clinical data workflows, data validation, and database lock processes

  • Ability to identify, troubleshoot, and resolve technical and system-related issues

Professional Skills

  • Excellent written and verbal communication skills

  • Strong attention to detail and analytical problem-solving abilities

  • Ability to manage multiple priorities and meet competing deadlines

  • Demonstrated leadership capability within cross-functional project teams

  • High level of initiative, accountability, and delivery focus


Regulatory & Quality Knowledge

  • Working knowledge of Good Clinical Practice (GCP) and applicable SOPs

  • Ability to interpret and contribute to internal policies and compliance frameworks

  • Quality-driven mindset with a strong commitment to accurate and timely data delivery


Working Conditions

  • Fully remote role with standard office environment requirements

  • Second-shift working hours (Afternoon schedule)

  • Occasional domestic or international travel may be required based on project needs


Why Join Thermo Fisher Scientific?

  • Work on global clinical trials with leading pharmaceutical and biotechnology sponsors

  • Be part of a high-performing, scientifically driven clinical research organization

  • Gain exposure to advanced EDC platforms and complex, multi-country studies

  • Access continuous learning, professional development, and long-term career growth

  • Competitive compensation, benefits, and a collaborative remote work culture