Title: Senior CDM Programmer – EDC
Location: Remote, India
Job Type: Full-Time
Category: Clinical Data Management / Clinical Research – Remote
Company Overview:
Join PPD® Clinical Research Services, a global leader in clinical trials and drug development, part of Thermo Fisher Scientific. We bring advanced scientific and clinical expertise to support life-changing therapies for some of the world’s most challenging health concerns. Our teams operate globally, leveraging technology-driven solutions to accelerate clinical research and improve patient outcomes.
Role Overview:
We are seeking a Senior CDM Programmer – EDC with extensive experience in Medidata Rave and Veeva Vault systems. The candidate will provide technical leadership for database development, data validation, and overall clinical data management activities. This role serves as a lead programmer on complex studies, collaborating with project teams and clients to ensure timely, high-quality deliverables.
Key Responsibilities:
Lead design, development, and testing of clinical trial databases in Medidata Rave and Veeva Vault.
Implement and validate edit checks, custom functions, and complex programming tasks.
Manage global libraries and ensure adherence to SDTM standards.
Coordinate multiple studies simultaneously, providing technical guidance and leadership to junior programmers.
Mentor and train team members on programming best practices, database development, and EDC processes.
Collaborate with project managers, clients, and cross-functional teams to meet project timelines and quality standards.
Troubleshoot database and programming issues, developing innovative solutions for complex data challenges.
Contribute to SOP development, departmental process improvements, and internal tool enhancements.
Provide input for client proposals, bidding processes, and knowledge sharing through publications or conference presentations.
Qualifications & Experience:
Bachelor’s degree in Life Sciences, Computer Science, or equivalent; advanced degrees preferred.
Minimum of 5+ years of experience as an EDC programmer, with hands-on expertise in Medidata Rave or Veeva Vault.
Strong experience with edit checks, custom functions, and clinical programming activities.
Proficiency in programming languages (C#, SQL) and relational database systems.
Experience with reporting tools such as Crystal Reports, SpotFire, and JReview.
Familiarity with GCP, clinical SOPs, and regulatory standards.
Demonstrated leadership, mentoring, and team management skills.
Excellent analytical, problem-solving, and organizational abilities.
Strong written and verbal communication skills; capable of working effectively in a multidisciplinary, remote team environment.
Skills & Competencies:
Advanced technical knowledge of EDC systems and clinical data management processes.
Ability to handle multiple projects with competing priorities and meet challenging deadlines.
Strong presentation, interpersonal, and collaboration skills.
Proactive in identifying opportunities for process improvement and system enhancements.
Why Join Us:
Work remotely in a globally recognized CRO, contributing to clinical trials that make a difference in patient outcomes.
Lead and mentor teams on complex EDC programming projects.
Access opportunities for professional development and career growth within Thermo Fisher Scientific.
Collaborate with experts in clinical data management, biostatistics, and project management.
Equal Opportunity Employer:
Thermo Fisher Scientific is committed to creating a diverse, inclusive, and equitable workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected status.
Apply Now: Advance your career as a Senior CDM Programmer – EDC and contribute to global clinical research excellence.
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Bangor | Brewer |New Jersey :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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