Senior CDM Programmer (EDC) – Clinical Research
Job ID: R-01335698
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Mode: Fully Remote
Location: India (Remote)
Shift: Second Shift (Afternoon)
Job Overview
Thermo Fisher Scientific, through its PPD® Clinical Research Services division, is seeking an experienced Senior CDM Programmer (EDC) to support global clinical trials across multiple therapeutic areas. This role is ideal for a technically strong EDC professional with deep expertise in Medidata RAVE and Veeva Vault EDC systems who can lead complex studies, mentor junior team members, and deliver high-quality data management solutions in a global CRO environment.
As a Senior CDM Programmer, you will provide technical leadership across database development, edit check programming, validation, and reporting while collaborating closely with cross-functional teams and global clients.
Key Responsibilities
Serve as the lead EDC programmer on assigned clinical studies of moderate to high complexity
Design, build, test, and maintain clinical trial databases using Medidata RAVE and/or Veeva Vault EDC
Develop and validate edit checks, custom functions, and advanced EDC configurations to support protocol requirements
Manage and support Global Libraries in alignment with SDTM standards
Provide hands-on technical leadership for database development, data validation, and system enhancements
Collaborate with project managers, data managers, statisticians, and client representatives to define timelines and deliverables
Lead multiple studies and clients simultaneously, adapting to evolving project and technology needs
Ensure programming deliverables meet quality, timeline, and contractual requirements
Research and resolve complex technical issues by applying new tools, programming techniques, and best practices
Train, mentor, and guide junior programmers and peers to strengthen team capability
Contribute to departmental initiatives, SOP development, and process improvement activities
Support reporting tool development and system troubleshooting in collaboration with IT teams
Provide technical input during bid development and proposal activities
Support knowledge sharing through internal initiatives and external industry publications or conference presentations, as applicable
Education & Experience Requirements
Bachelor’s degree in Life Sciences, Computer Science, Clinical Research, or a related discipline
Minimum 5+ years of hands-on experience as an EDC Programmer within a CRO, pharmaceutical, or biotechnology environment
Proven experience working with Medidata RAVE and/or Veeva Vault EDC platforms
Equivalent combinations of education, training, and relevant experience may be considered
Required Skills & Competencies
Strong expertise in EDC programming, including edit checks, custom functions, and database configuration
Proficiency in SDTM standards and global library management
Experience with one or more programming languages and relational database systems (RDBMS)
Working knowledge of tools such as SQL, C#, Crystal Reports, Spotfire, and JReview
Strong understanding of GCP, regulatory requirements, and applicable SOPs
Excellent written and verbal communication skills with strong documentation abilities
Demonstrated leadership capability and experience mentoring junior team members
Strong organizational and time-management skills with the ability to manage multiple priorities
Analytical mindset with proven problem-solving and troubleshooting skills
Ability to work independently while collaborating effectively within global, cross-functional teams
Why Join Thermo Fisher Scientific
Work on global clinical trials across diverse therapeutic areas and study phases
Gain exposure to complex EDC builds and advanced clinical programming environments
Strengthen leadership, technical, and project management capabilities
Collaborate with international sponsors, CRO teams, and technology partners
Access continuous learning opportunities within a mature and globally recognized CRO model
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is a global leader in serving science, enabling customers to make the world healthier, cleaner, and safer. With annual revenue exceeding $44 billion and a global workforce of more than 90,000 professionals, the company delivers innovative technologies and clinical research services through trusted brands including PPD®, Thermo Scientific, Applied Biosystems, Invitrogen, and Patheon.
Thermo Fisher Scientific is an equal opportunity employer and is committed to diversity, inclusion, and professional development.
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