Sr CDM Programmer II (Rave CF)
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety StandardsJob Description
The Senior CDM Programmer II provides technical leadership in clinical data management activities
including database development edit check programming data validation and reporting. This role
serves as a subject matter expert within a multi-disciplinary project team ensuring deliverables are
completed on time within scope and in compliance with applicable standards and regulations. The
position also supports process improvement initiatives and contributes to the development of tools
and standards that enhance operational efficiency.
What Youll Do:
Design build test and maintain clinical study databases and edit checks.
Configure and develop clinical studies in Medidata Rave including eCRF design and
deployments.
Develop test and validate Rave Custom Functions using C#.
Configure and manage the Rave Lab Module including lab data imports and reconciliation.
Define and import data into EDC systems.
Develop and test listings and reports to support data review.
Create automation tools and scripts using Python for data validation and reporting.
Troubleshoot system issues and collaborate with cross-functional teams for resolution.
Provide technical leadership and mentor junior programmers.
Participate in process improvements bid defenses and SOP updates as needed.
Education & Experience Requirements:
MS/MA degree in computer science statistics biostatistics mathematics or related field and at least 3 years of experience that provides the knowledge skills and abilities to perform the job requirements or Bachelors degree in computer science statistics biostatistics mathematics or related field or equivalent and relevant formal academic / vocational qualification
At least 5 years of experience that provides the knowledge skills and abilities to perform the job requirements.
Years of experience refers to typical years of related experience needed to gain the required knowledge skills and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge Skills Abilities:
Strong experience with Medidata Rave (study build edit checks validation deployment).
Advanced experience developing Rave Custom Functions.
Experience with Rave Lab Module and external lab data integration.
Strong proficiency in C# programming language.
Proficiency in Python for automation and data processing.
Good understanding of AI-powered tools such as ChatGPT and similar generative AI
platforms for productivity automation and process optimization.
Experience with relational database systems (RDBMS).
Proficiency with SAS SQL Crystal Reports SpotFire and JReview.
Strong understanding of GCP and clinical data management processes.
Strong analytical problem-solving and communication skills.
Ability to manage multiple priorities in a fast-paced environment.
Working Conditions and Environment:
- The standard working hours are from 1:00 PM to 10:00 PM IST.
- Employees have the flexibility to choose between office remote or hybrid work options.
Why Join Us
Join us in our mission to make the world healthier cleaner and safer by successfully implementing your expertise in data management. Apply today and become part of our ambitious team at Trialmed (a global site network and the early phase clinical solution for PPD the clinical research business of Thermo Fisher Scientific Inc.).
Apply today to help us deliver tomorrows breakthroughs.
Required Experience:
Senior IC
About Company
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