Senior CDM Programmer (EDC) – Clinical Research
Location: Fully Remote – India
Job Type: Full-Time
Job ID: R-01335698
Category: Clinical Research / Clinical Data Management
Work Schedule: Second Shift (Afternoon Shift)
About the Organization
Our Clinical Research Services team plays a critical role in accelerating the delivery of life-saving therapies to market. As part of a leading global Contract Research Organization (CRO), the team brings deep scientific, clinical, and technical expertise to the development of innovative drugs addressing complex global health challenges. The Clinical Research professionals supporting the PPD® clinical research portfolio work at the forefront of data-driven clinical development, ensuring quality, compliance, and operational excellence across global trials.
Position Summary
The Senior CDM Programmer (EDC) will provide technical and functional leadership in clinical data management, with a strong focus on Electronic Data Capture (EDC) systems. This role involves hands-on database development, validation, and programming activities using industry-leading platforms such as Medidata Rave and Veeva Vault. The position requires leading moderate to complex clinical studies, collaborating closely with cross-functional project teams and client stakeholders, and mentoring junior programmers to deliver high-quality clinical data solutions.
Key Responsibilities
Lead and execute EDC programming activities, including database design, development, testing, and validation for clinical trials of moderate to high complexity.
Serve as the lead EDC programmer on assigned studies, partnering with project managers, clinical teams, and client representatives to define project goals and timelines.
Provide technical expertise in Medidata Rave and Veeva Vault EDC systems, managing complex study configurations and requirements.
Design, build, and maintain edit checks, custom functions, and advanced database logic to ensure data quality and regulatory compliance.
Manage and support global libraries in alignment with SDTM standards.
Oversee multiple studies and clients concurrently, demonstrating flexibility and adaptability to new tools, platforms, and evolving project needs.
Ensure all deliverables meet quality standards, contractual requirements, and established timelines.
Identify and resolve technical and operational issues through independent research and application of advanced programming and data management expertise.
Provide leadership and mentorship to junior programmers, supporting skill development and consistent delivery of best practices.
Contribute to departmental initiatives, SOP development, process optimization, and participation in bid defense activities.
Collaborate with IT teams to troubleshoot system issues and support the development and validation of reporting tools and standard applications.
Support scientific visibility by contributing to industry publications, conference presentations, and knowledge-sharing initiatives.
Experience and Qualifications Required
Bachelor’s degree or equivalent formal academic or vocational qualification in a relevant discipline.
Minimum 5+ years of hands-on experience as an EDC or CDM Programmer within a clinical research or CRO environment.
Proven experience working with Medidata Rave and/or Veeva Vault EDC platforms.
Strong expertise in edit checks, custom functions, and clinical database programming activities.
Proficiency in one or more programming languages and strong working knowledge of relational database management systems (RDBMS).
Experience using programming and reporting tools such as C#, SQL, Crystal Reports, Spotfire, and JReview.
Demonstrated understanding and application of Good Clinical Practice (GCP) guidelines and applicable SOPs.
Strong written, verbal, presentation, and interpersonal communication skills.
Proven leadership capability, with experience mentoring team members and working effectively in multidisciplinary project teams.
Excellent organizational and time management skills, with the ability to manage multiple studies and competing deadlines.
Strong analytical, problem-solving, and decision-making abilities, with a continuous improvement mindset.
Why Join Us
Fully remote role offering flexibility and work-life balance within a global clinical research environment.
Opportunity to work on complex, high-impact clinical trials supporting innovative therapies.
Collaborative, performance-driven culture with opportunities for professional growth and leadership development.
Exposure to global clients, advanced EDC technologies, and evolving clinical data standards.
How to Apply
Qualified professionals interested in advancing their career in clinical data management are encouraged to apply through the official careers portal. Applications will be reviewed on an ongoing basis.
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