Job Title: Senior CDM Programmer (EDC)
Location: Remote, India (Fully Remote)
Job Type: Full-Time | Second Shift (Afternoons)
Category: Clinical Research
Industry: Global CRO / Clinical Trials
Platform: thepharmadaily.com
We are hiring an experienced Senior Clinical Data Management (CDM) Programmer – EDC to join a leading global Contract Research Organization (CRO). This fully remote role is ideal for professionals with strong hands-on expertise in Medidata Rave and Veeva Vault EDC systems, who can provide technical leadership across complex global clinical trials.
As a Senior CDM Programmer, you will act as a technical lead on multiple studies, collaborate closely with cross-functional project teams and clients, and ensure high-quality database development, validation, and delivery in compliance with regulatory and industry standards.
Serve as the lead EDC programmer for medium to high-complexity clinical studies.
Design, build, test, and maintain EDC databases, edit checks, and custom functions.
Provide advanced technical support for Medidata Rave and Veeva Vault EDC platforms.
Manage and implement Global Libraries in alignment with SDTM standards.
Lead multiple studies and clients simultaneously, adapting to new tools and study requirements.
Ensure timely, high-quality deliverables in accordance with project timelines and contractual obligations.
Identify, analyze, and resolve complex programming and system-related issues.
Mentor, train, and guide junior programmers and peers.
Contribute to process improvements, SOP development, and departmental initiatives.
Support bid proposals and participate in system troubleshooting with IT teams.
Promote organizational visibility through publications, presentations, or conference participation where applicable.
Minimum 5+ years of experience as an EDC/CDM Programmer in clinical research.
Proven hands-on experience with Medidata Rave and/or Veeva Vault EDC.
Strong expertise in edit checks, custom functions, and database validation.
Experience working on global clinical trials within a CRO environment.
Bachelor’s degree in Life Sciences, Computer Science, Biotechnology, Statistics, or a related field
Equivalent education combined with relevant professional experience will be considered
Strong understanding of clinical data management processes and GCP guidelines
Proficiency in SQL, C#, relational database systems (RDBMS)
Experience with tools such as Crystal Reports, Spotfire, JReview is preferred
Excellent analytical, problem-solving, and troubleshooting abilities
Strong written, verbal, and presentation skills
Demonstrated leadership, mentoring, and cross-functional collaboration skills
Ability to manage multiple priorities and tight deadlines in a fast-paced environment
Fully remote opportunity with a globally recognized CRO
Leadership role with exposure to international clinical trials
Strong career growth and learning opportunities
Collaborative, innovation-driven work culture
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