and experience. • Knowledge of database set-up and report publishing requirements. • Advanced knowledge of technical and regulatory requirements related to the role. • Knowledge of CDISCstandards (e.g., CDASH, SDTM, ADaM) and industry best practices. • Advanced knowledge and experience of clinical drug development or healthcare. more »
with multiple functional areas across the company. Skills & Requirements: Advanced degree (MSc or PhD). Proficiency in statistical programming, particularly SAS. Detailed knowledge of CDISCstandards (SDTM, ADAM). Excellent communication skills, both written and verbal, with the ability to communicate complex statistical concepts to non-statistical audiences. Ability to more »
the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines. 2. Implement and follow the latest versions of CDISC, FDA Guidelines, GCP and other industry standards. 3. Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database more »
Mathematics, Computer Science or similar). 3-5 years’ experience with SAS® programming within the clinical industry. Working experience of using and implementing the CDISC SDTM and CDISC ADaM standards. At least 2 years’ experience in leading studies from data extraction through to TFL outputs. Desirable Experience with R or more »
Statistical Programmer - multiple levels Home based #Oncology focused Our client, a global mid-size Pharma, have extended reputation in key therapeutic indications e.g. oncology, rheumatology, rare diseases, etc. and has supported the development of some of the most successful products. more »
Programming experience within the pharmaceutical industry essential. Excellent knowledge of SAS essential and R or Python advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinicaldatastandards (CDISC), TLFs, and submission guidelines Exposure to working with clinical datasets, statistical methodology, and CSR/submission deliverables. more »
the study through to final delivery of clinical datasets. Providing SAS programming support through all phases of the projects along with detailed knowledge of CDISC with experience of mapping and programming SDTM standard datasets is essential. This is a hybrid role and will initially require more office presence, gradually transitioning … planning of assigned projects. Provide hands on technical data management expertise and SAS programming support through all phases of the projects following industry standards (CDISC), from database build through to delivery of mapped datasets. Support projects from both the Clinical Site data perspective, as well as the Data Management vendor … of end to end Clinical trial and Project Data Management processes, as well as extensive experience in the Data Management industry Detailed knowledge of CDISC with experience mapping and programming SDTM standard datasets Flexible and adaptive approach, being able to rapidly re-prioritise whilst maintaining a clear vision, as well more »
