Transforming clinical data starts with you!

The Clinical Data Manager I (CDM I) provides operational and project-specific support for clinical data management activities. The CDM serves as the primary point of contact for sponsors, sites, and vendors regarding data-related issues and ensures compliance with Good Clinical Practices (GCP), ICH guidelines, and company SOPs. This role requires strong attention to detail, excellent communication skills, and the ability to manage multiple projects simultaneously. 

The Clinical Data Manager II independently manages moderate to complex clinical studies, serving as the primary data management lead for sponsors, sites, and vendors. This position is responsible for overseeing data collection, database setup, maintenance, validation, and closeout activities to ensure high-quality deliverables within budget and timelines.  

The primary responsibilities of this position are to provide leadership in planning and conducting data analyses in clinical studies, and participate in planning and data analyses for regulatory submission. 

The primary responsibilities of this position are to provide statistical consulting to clients in the biotech/pharmaceutical industry in their drug development programs with a focus on protocol/study design, analysis planning, and regulatory submission strategies.    

The primary responsibilities of this position are to assist with study level statistical related activities, particularly to write statistical analysis plans, prepare mock tables/figures/listings, and generate statistical analyses for clinical studies conducted by pharmaceutical and biotech companies.