Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Join Us as a Sr CDM Programmer II - Make an Impact at the Forefront of Innovation
The Sr CDM P II works with clinical data management systems and programming tools to provide technical leadership in data management activities and deliverables including, but not limited to, database development and data validations. The Sr CDM P II acts as a leader within a multi-disciplinary project team to complete assigned tasks on time and within budget and serves as technical knowledge expert and provides leadership across departmental processes and projects. The role involves supporting management in oversight of study day to day activities and identification/creation of needed tools and process improvements to increase efficiencies within the project and the team.

We are presenting an outstanding opportunity to join Thermo Fisher Scientific as a Sr. CDM Programmer (Python). In this role, you will play a key part in systems analysis, development, testing, and support of moderately complex technical information system components, with a strong focus on Python-based backend services and Clinical data processing solutions.

• Demonstrate a strong client-focused approach with excellent communication and interpersonal skills, effectively collaborating with cross-functional stakeholders

• Exhibit the ability to manage multiple priorities, ensuring timely delivery while maintaining a high level of accuracy and attention to detail

• Utilize advanced Python expertise for backend development, automation, and large-scale data processing

• Hands-on experience in clinical data preparation with domain knowledge is highly desirable

• Demonstrated expertise in SDTM, including toxicity grading (Grade Tox), AE severity classification, and associated data standards

• Design and develop Python-based solutions for data processing, workflow automation, and seamless integration with modern data platforms

• Perform data analysis, validation, and reconciliation across multiple data sources to ensure data integrity and consistency

• Support the migration and modernization of legacy SAS workloads to cloud-based or Python-driven frameworks

• Develop and maintain Spotfire dashboards for clinical data review, enabling real-time insights into safety and efficacy data while ensuring compliance with SDTM standards

• Collaborate with clinical, data management, and biostatistics teams to support data-driven decision-making through effective visualization and analytics

• Conduct system analysis and prepare comprehensive technical documentation, including requirements, specifications, test plans, and user manuals

• Analyze, troubleshoot, and resolve production and support issues, providing guidance and training to business users as needed

• Leverage AI-assisted development tools to enhance coding efficiency, improve code quality, and streamline testing and documentation processes