Quanticate
Biotech
ClinicalDataManagementProgrammer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Data Management Programmer at Quanticate. Skills: Clinical Data Management, EDC platforms, Clinical programming. Support clinical studies. Perform technical tasks”
Industry & Context.
Resolve programming defects
What They're Looking For.
Must Have
Minimum 3+ years of experience in Clinical Data Management, Experience supporting clinical trials, Experience working with EDC systems, Proficiency in Microsoft Office Suite
Nice to Have
Master's degree preferred, Experience with PL/SQL, Experience with SAS, Experience with C#, Experience with VB, Experience with application programming, Experience with system integrations, Experience in a matrix organisational structure
What You'll Do.
Support clinical studies
Perform technical tasks
Perform programming tasks
Implement edit checks
Design data validations
Implement data validations
Implement derivations
Set up electronic data imports
Manage electronic data imports
Validate electronic data imports
Set up electronic data exports
Manage electronic data exports
Validate electronic data exports
Prepare documentation
Conduct quality control checks
Support reporting programming
Ensure timely delivery
Resolve programming defects
Contribute to process improvements
Contribute to standardisation
Contribute to best practices
Manage User Access Management
Maintain related documentation
Collaborate with cross-functional teams
Support system integrations
Support system updates
Support UAT activities
Ensure compliance with study standards
Ensure compliance with SOPs
Ensure compliance with regulatory requirements
How You'll Work.
Team & Collaboration
Cross-functional teams; External stakeholders
Communication Scope
Written communication; Verbal communication
Full Job Description
Join a dynamic and growing clinical research organisation at the forefront of data-driven innovation in clinical trials. We are committed to delivering high-quality, reliable data solutions that accelerate drug development and improve patient outcomes worldwide. Our collaborative, fast-paced environment empowers talented professionals to make a meaningful impact while continuously developing their skills. This is an exciting opportunity for a detail-oriented and technically strong CDM professional to expand their expertise, contribute to process improvements, and work with industry-leading tools in a highly collaborative environment. ### **What You’ll Do** * Work as a Clinical Data Management (CDM) Programmer supporting clinical studies. * Perform technical and programming tasks for assigned projects, ensuring high data quality and compliance. * Design and implement complex edit checks, data validations, and derivations. * Set up, manage, and validate electronic data imports and exports. * Prepare datasets and documentation for study completion and regulatory submissions. * Conduct quality control (QC) checks on programming outputs. * Support reporting programming and ensure timely delivery against project schedules. * Monitor systems for workflow alerts, performance issues, and resolve programming defects. * Contribute to process improvements, standardisation, and best practices. * Manage User Access Management (UAM) for EDC studies and maintain related documentation. * Collaborate with cross-functional teams and support system integrations, updates, and UAT activities. * Ensure compliance with study standards, SOPs, and regulatory requirements. ### **What You’ll Gain** * Hands-on experience with leading EDC platforms and advanced clinical programming tools. * Exposure to global clinical trials and collaboration with sponsors and cross-functional teams. * Opportunities to contribute to process improvements and innovation initiatives. * Continuous learning through t
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