Maintains an overview of program status and proactively communicates progress, risks, or changes that may impact quality, timelines, and budget. Reviews plans and provides CDM expertise during protocol design, study start-up, and conduct phases of studies. Ensures consistency within the program and develops standard methodologies within CDM. Leverages standards for data collection and cleaning to ensure quality results and implement timely delivery. Requirements:
Bachelor's degree in Mathematics, Science, or a related field. Minimum 12 years of clinical data management experience in biotechnology, pharmaceutical, or health-related industries. This role involves collaborating with senior-level management, external vendors, collaboration partners, and clinical study personnel to drive clinical research project initiatives and department objectives. The salary range for this position is between $150,000 and $250,000 per year, depending on location and experience.