The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation
The Central Monitor (CM) will perform centralized and prompt monitoring activities for Phase I-IV clinical research and/or non-interventional studies (NIS) in accordance with project plans, the protocol, ICH-GCP, and/or all applicable local and federal regulatory requirements as
Medical Oversight : - Provide clarity on general protocol questions, and medical guidance for protocols as required. - Serve as medical expert providing guidance on patient eligibility, and investigational product related questions. - Document contacts in