3 of 3 Good Clinical Practice Jobs in the UK excluding London

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home … Program quality control checks for source data and reporting data issues Interpret project level requirements and develop programming specifications Write programming code following established Good Programming Practices Program ADaM datasets Program to create statistical analysis tables, listings, and figures Validate datasets and all statistical outputs per prescribed gate checks … Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines Use and promote the use of established standards, SOPs, and standard methodologies Export data and clinical study report materials Provide training and mentoring to team members and department staff You more »

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home … Program quality control checks for source data and reporting data issues Interpret project level requirements and develop programming specifications Write programming code following established Good Programming Practices Program ADaM datasets Program to create statistical analysis tables, listings, and figures Validate datasets and all statistical outputs per prescribed gate checks … Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines Use and promote the use of established standards, SOPs, and standard methodologies Export data and clinical study report materials Provide training and mentoring to team members and department staff You more »

focus on treating, curing, and preventing some of the most devastating and complex diseases of our time. Within Enabling Business Information Solutions (EBIS), the Clinical Trial Management Solutions business is recruiting for a Trial Master File (TMF) Analyst to join our Trial Master File (TMF) Center of Excellence (COE … Education : A bachelor's degree is required, preferably in health, science, or information technology. Experience : At least 3 years in the pharmaceutical industry or clinical trials. Candidates should have strong technical expertise, with proficiency in electronic records systems (particularly eTMF), IT tools, data warehouses, and, ideally, database administration. Familiarity … Artificial Intelligence (AI) is a plus. An understanding of TMF content management, clinical trial conduct, drug development processes, and regulatory standards (ICH/GCP) is advantageous. Experience with audits, inspections, and implementing quality metrics to support decision-making is highly desirable. Good communication, problem-solving, and organizational skills more »