Sr. CDM Programmer (RAVE CF)
Company: Thermo Fisher Scientific (PPD Clinical Research Services)
Location: Bangalore, India | Fully Remote
Job Type: Full-Time | Remote
Work Schedule: Standard (Mon–Fri)
Experience: Typically 5+ Years (Clinical Data Management / EDC Programming)
Qualification: Bachelor’s Degree in Life Sciences, Computer Science, or Related Discipline
Salary Range: Not Specified
Job Overview
Thermo Fisher Scientific is seeking a Sr. CDM Programmer with strong expertise in Electronic Data Capture (EDC) systems, particularly Medidata Rave and Veeva Vault, to support clinical trial data management and database programming activities.
The Sr. CDM Programmer will work on database development, data validation, and programming deliverables while providing technical leadership across clinical studies. The role involves working closely with cross-functional teams and clients to design, build, and maintain clinical trial databases, ensuring data accuracy, compliance, and efficiency.
This position plays a critical role in managing complex studies, improving data management workflows, and leading programming activities to support high-quality clinical trial execution.
Key Responsibilities
1. Clinical Database Development & EDC Programming
Design, build, and test clinical trial databases using EDC systems.
Work extensively with:
Medidata Rave
Veeva Vault
Develop and implement edit checks and custom functions for data validation.
Handle complex study requirements within EDC platforms.
Ensure database structures align with protocol and study requirements.
2. Data Validation & Quality Management
Perform data validation to ensure accuracy, completeness, and consistency.
Develop and execute edit checks for clinical datasets.
Ensure compliance with SDTM standards and global data standards.
Maintain data integrity across multiple clinical studies and systems.
Support quality control and audit readiness processes.
3. Study Leadership & Project Management
Act as lead programmer on moderate complexity clinical studies.
Collaborate with project teams and clients to define timelines and deliverables.
Manage multiple studies and clients simultaneously.
Ensure deliverables meet timelines, quality standards, and contractual requirements.
Adapt to new tools and technologies based on project needs.
4. Programming & Technical Expertise
Utilize programming tools such as:
C#
SQL
Crystal Reports
SpotFire
JReview
Work with relational database systems (RDBMS) for structured data handling.
Develop and optimize programming solutions for clinical data workflows.
Troubleshoot and resolve technical issues related to data systems and programming.
5. Process Improvement & Innovation
Identify opportunities to improve data management and programming processes.
Contribute to development of reporting tools and standard applications.
Support automation and efficiency improvements in workflows.
Participate in departmental and organizational process initiatives.
6. Team Leadership & Mentoring
Train, mentor, and guide junior programmers and team members.
Coordinate team activities and ensure alignment with project goals.
Provide technical leadership within multidisciplinary clinical teams.
Promote knowledge sharing and skill development within the team.
7. Compliance, Documentation & Governance
Ensure compliance with GCP guidelines and internal SOPs.
Maintain proper documentation for programming activities and deliverables.
Support SOP development and updates.
Provide input during bidding and proposal processes.
Collaborate with IT teams to resolve system-related issues.
Required Skills
EDC & Clinical Data Management
Strong experience with:
Medidata Rave
Veeva Vault
Expertise in edit checks, custom functions, and database programming.
Knowledge of SDTM standards and clinical data workflows.
Understanding of clinical trial data management processes.
Programming & Technical Skills
Proficiency in:
C#
SQL
Experience with tools such as:
Crystal Reports
SpotFire
JReview
Strong understanding of relational databases (RDBMS).
Ability to troubleshoot and optimize programming solutions.
Problem Solving & Analytical Skills
Strong analytical and problem-solving abilities.
Ability to manage complex programming and data challenges.
Attention to detail in data validation and system design.
Capability to resolve technical issues efficiently.
Project Management & Collaboration
Ability to manage multiple studies and deadlines.
Strong organizational and time management skills.
Effective communication with cross-functional teams and clients.
Ability to work in multidisciplinary and global environments.
Leadership & Communication
Demonstrated leadership and mentoring ability.
Strong interpersonal and presentation skills.
Ability to guide and support junior team members.
Positive attitude and collaborative work approach.
Preferred Qualifications
Experience in pharmaceutical or CRO clinical research environment.
Hands-on experience with EDC systems and clinical trial databases.
Familiarity with regulatory standards and clinical data guidelines.
Experience in process improvement and automation initiatives.
Participation in industry conferences or publications is a plus.
Key Competencies
Clinical database development and EDC programming
Data validation and quality management
Clinical trial data standards (SDTM)
Programming and database management
Technical leadership and mentoring
Process improvement and workflow optimization
Cross-functional collaboration
About the Company
Thermo Fisher Scientific is a global leader in scientific services and technologies, supporting research, drug development, and healthcare innovation worldwide.
Through its clinical research division, PPD Clinical Research Services, the organization provides end-to-end clinical trial services including clinical operations, data management, regulatory affairs, and medical writing.
Operating in more than 100 countries with over 100,000 employees globally, the company partners with pharmaceutical and biotechnology organizations to accelerate the development of innovative therapies and deliver life-changing treatments to patients around the world.
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