ClinChoice Benefits Overview

Lead end-to-end statistical programming for oncology clinical trials: develop and validate SDTM/ADaM datasets, produce TLFs, support integrated analyses (ISS/ISE), manage study timelines and vendors, and prepare submission-ready outputs (define.xml, annotated CRFs, reviewer guides) for regulatory submissions (FDA/EMA/PMDA).

Lead cross-functional teams to manage complex clinical trials across various health sectors while ensuring compliance with GCP and regulatory standards.

As a Clinical Project Manager II, you will oversee execution and delivery of clinical studies, manage vendor activities, and track project progress, focusing on oncology and hematology trials.