Requirements: B.Sc., M.Sc., or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields Advanced SAS macro programming experience is required for the development o...
Summary We are seeking a highly skilled Data Integrity SME with a strong Quality Assurance background and hands-on experience in analytical equipment documentation within the pharmaceutical industry. The ideal candidate will ensure data in...
Summary: We are seeking a highly skilled and detail-oriented Supplier Quality Engineer to join our team. The ideal candidate will have a strong background in medical device supplier quality, with hands-on experience in supplier qualificati...
Responsibilities: In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key m...
Responsibilities: Accurate and timely registration of adverse event and product quality report from initial receipt to data entry within required timeframes. Performing Quality Review of external provider's reconciliation tasks for Clini...
Job Description: The Lead Systems Designer leads a couple of cross-functional program teams (7T Program and 3T MAGNUS (Head Only Scanner)) Programs to deliver the technical content, performance, intellectual property, and quality deliverab...
Job Description: Experienced with lab settings for daily support of safety, lab organization and lab upkeep (receiving materials, waste management, etc.). Role requires support of multiple lab areas at multiple sites. Experience with anal...
Job Description: Responsible for supporting Process Chemistry and Engineering operations within the Pharmaceutical Products Group - API at Client Lake County. The Lab Manager will work directly with organizing laboratory spaces, managing c...
Responsibilities: Lead the development, validation, and documentation of CDISC-compliant SDTM and ADaM datasets for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings, and f...
Responsibilities: Provide leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection, budgeting, resource planning, vendor oversight, EDC build and study timelin...