Jobs at ClinChoice

Lead and support clinical statistical programming: develop, validate, and maintain SAS programs; create SDTM/ADaM datasets and TLFs; collaborate with Biostatistics, Data Management, and Clinical teams; ensure deliverable quality and timelines; review specifications, participate in study planning, and support regulatory submission activities.

Develop and validate SDTM and ADaM datasets using R per CDISC standards, support TLF generation in R or SAS, perform QC and reconcile data issues, collaborate with biostatistics and clinical teams, and contribute to automation and reproducible workflows for regulatory submissions.

Lead statistical activities for oncology clinical trials, providing strategic input, developing analysis plans, and mentoring junior statisticians. Collaborate on regulatory submissions and ensure compliance with standards.

Manage biometrics project teams across Data Management, Biostatistics, Statistical Programming, and Medical Writing from study start-up through closeout. Serve as primary client/vendor liaison, coordinate meetings, timelines, milestones, and action items, manage project financials and contracts support, identify risks and change orders, ensure training completion, support business development (RFPs/RFIs), and escalate or resolve issues.

The Business Development Director is responsible for driving growth by securing new clients and expanding services, managing the full sales lifecycle, and maintaining relationships with key stakeholders in the life-sciences industry.

Lead statistical strategy and deliverables for clinical trials (primarily immunology), author and review SAPs and ADS, interpret analysis outputs, ensure regulatory compliance, collaborate with clinical, programming, data management and regulatory teams, oversee/mentor statisticians and programmers.

Seeking a Statistical Programmer II/III to develop and maintain statistical programs primarily using R and SAS for clinical trial data analysis, collaborating with clinical teams to ensure compliance and support submissions.

The Senior Statistical Programmer will program and validate datasets for clinical trials, oversee deliverables, manage projects, and ensure compliance with industry standards. Requires strong skills in SAS and R for statistical programming.

Lead analytical efforts in Real World Data research, develop specifications and methodologies, manage projects, and communicate findings to stakeholders.