ClinChoice

Compliance

• Support Clients France Regulatory Affairs (RA) team
• Review and approve promotional materials for regulatory compliance
• Evaluate artworks and packaging to ensure alignment with applicable regulations
• Conduct product claim assessments in accordance with EU and French cosmetic/commodities legislation
• Provide support in responding to health authority queries and inspections
• Collaborate closely with marketing, legal, and regulatory stakeholders
• Stay current with regulatory developments, particularly in France and the EU

Regulatory Affairs Consultant

Data Scientist

• Collaborate with Data Management teams to design and implement Data Transfer Specifications (DTS) aligned with client requirements
• Build and maintain ETL pipelines to automate extraction, transformation, and loading of data from multiple EDC platforms (Rave, Veeva, Medrio)
• Develop automation scripts in Python to streamline dashboard refreshes and reporting
• Design and deploy interactive Power BI dashboards integrating EDC systems and external sources (labs, MRI, ECG)
• Construct robust data models to support study-level and subject-level analysis
• Ensure data harmonization, normalization, and validation across datasets
• Apply advanced statistical methods and visualization techniques to analyze complex clinical datasets
• Partner with Data Managers to create tools for eCRF specification generation and customization
• Design and implement relational databases to optimize data storage, retrieval, and integration
• Develop user-friendly web interfaces (HTML, CSS, JavaScript) for internal tool accessibility
• Represent the Data Science team in client-facing meetings and collaborate with business development to identify data science opportunities

Senior Data Scientist

Director

• Lead and oversee statistical programming activities to support clinical trial projects
• Manage programmers and CROs and provide statistical programming oversight to vendors
• Review and validate datasets and TFLs programmed by vendors
• Support building programming processes for clinical studies and regulatory submissions
• Collaborate with Biostatistics, Data Management, Clinical Operations, Regulatory, Pharmacovigilance and other functions to deliver timely, high-quality data deliverables
• Develop and implement data review/reporting tools and other statistical applications as appropriate
• Review study documents (SAP, DMP, CRF, annotated CRF, TFL specifications) and provide expert feedback
• Build, mentor and manage a team of programmers to support clinical trials and pipelines
• Generate ad hoc analyses on an ongoing basis

Associate Director, Programming

Software Engineer

• Support Programming deliveries of a clinical study or project
• Implement statistical programming aspects of the protocol and the clinical development program
• Ensure high quality is built into own deliverables and those of other programmers
• Program independently with high efficiency and quality
• Write and/or implement specifications and oversee completeness of relevant documentation
• Contribute to development of best practices to improve quality, efficiency, and effectiveness
• Ensure compliance with standards and automation usage
• Plan and support team activities and tasks
• Communicate and escalate risks within assigned studies and/or projects
• Work proactively with study team members including Statistician, Lead Programmer, Data Manager and Study Leader
• Act as a client-facing consultant establishing a high-trust environment with client counterparts

Principal Statistical Programmer Consultant – Oncology

• Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings
• Produce data listings, summary tables, and graphics for interim and final analyses
• Integrate data across studies within a project and validate analysis datasets
• Test, document, review, and validate all programs according to department guidelines
• Coordinate data transfer and programming standards with CROs and vendors and validate vendor-delivered TFLs and datasets
• Collaborate with other Biometrics functions on clinical trial data analysis activities
• Execute ad-hoc requests, manuscripts, posters, and presentations
• Serve as client-facing principal statistical programming consultant working directly for a single sponsor while supported by ClinChoice

Principal Statistical Programmer Consultant

• Lead and support all statistical programming activities aligned with project strategies
• Use R to create high-quality clinical deliverables and validate outputs using SAS
• Develop Shiny Apps, and R packages; work on modern R framework for app building
• Develop Tables, Listings, and Figures (TLFs) using R
• Author and maintain reusable R macros/functions
• Validate R-based outputs and deliverables against SAS results or legacy code
• Customize outputs and visualizations based on statistical analysis plans and audience requirements
• Take ownership of programming deliverables for clinical studies or projects
• Actively contribute to process improvement, programming standards, and best practices
• Ensure compliance with CDISC standards and maximize automation and reusable code
• Coordinate programming activities, anticipate resource needs, and support timelines
• Proactively identify and communicate risks or issues related to assigned studies/projects

Principal R Programmer

• This position provides high quality statistical programming deliverables for global stakeholders in Early Development Statistics and PK/PD Modeling and Simulation spanning all client therapeutic areas except oncology.
• The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve required data, transform data into analysis/modeling datasets, and develop tables, listings and figures according to statistical/modeling analysis plan.
• The senior programmer will be a key collaborator with statisticians, modelers, and colleagues in other related function areas.
• Prepare compliant programming code for regulatory submissions including analysis/modeling datasets, tables, listings, figures and associated documentation
• Ensure programmatic traceability from data source to analysis/modeling result
• Support the development of programming standards to enable efficient and high-quality production of programming deliverables.