Teams at ClinChoice

Leads statistical programming for clinical trials, developing and reviewing SAS programs, datasets, tables, listings, and figures. Supports SDTM/ADaM standards and regulatory submissions, reviews specifications and outputs, manages deliverables and timelines, collaborates with clinical teams, and provides technical guidance and mentorship to statistical programmers. Requires strong knowledge of clinical development, CDISC, ICH, Good Clinical Practices, and regulatory requirements.

Lead statistical activities for clinical studies, including protocol development, sample size calculations, randomization, statistical analysis plans, data quality oversight, and reporting. Ensure the validity, accuracy, consistency, and timeliness of analyses, tables, figures, listings, and statistical methods sections. Provide statistical guidance, mentor junior statisticians, coordinate assignments, review work, and support high-quality delivery across pharmaceutical, biotechnology, medical device, and consumer health projects.

Leads statistical activities for clinical trials across pharmaceutical, biotech, medical device, and consumer health projects. Acts as lead statistician, overseeing statistical strategy, SAPs, analysis database specifications, clinical study report sections, output interpretation, quality, and regulatory compliance. Collaborates with clinical, programming, data management, and regulatory teams; guides statistical programmers; communicates results and risks to technical and non-technical stakeholders; and ensures adherence to FDA, ICH, GCP, and company SOPs.