3 of 3 Good Clinical Practice Jobs in Surrey

Management Systems at MedPharm. The role is responsible for supporting compliance with Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), applicable regulatory requirements and internal quality procedures through the review of quality documentation, management of quality systems … metric reporting and trend analysis. General Build effective working relationships with internal departments, clients and external service providers. Maintain current knowledge of applicable GMP, GCP, GLP and regulatory requirements. Perform other duties appropriate to the position as requested by QA Management Key Relationships Heads of Departments Senior Management Production Pharmaceutical ...

requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Responsibilities: Responsible for supporting the Programming deliveries of a clinical study or project. Implements statistical programming aspects of the protocol and the clinical development program. Ensures high quality is built into own deliverables … Data Manager and Study Leader. Education and Experience: Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have ...

execution of programs in statistical programming languages within project. Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations. Create complex programs that meet regulatory and company standards to permit efficient programming, reporting, and review, utilizing statistical programming languages (e.g … relationship skills including consultative and relationship management skills. Full understanding and knowledge relevant to statistical programming. Full understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device setting. Strong problem-solving, organizational, analytical and critical thinking skills. Experience working in clinical ...