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 »
equivalent in computer science, mathematics, statistics, life sciences or related field(s). Excellent SAS programming skills (BASE, MACRO, GRAPH). Excellent knowledge of CDISC standards. Statistical Programming experience within a CRO Pharmaceutical/Healthcare/Biotechnology industries. Experience in statistical programming initiatives, and development of processes. Knowledge and experience 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 »
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 »
industry. - Knowledge of running numerous projects at once - including Phase II and/or Phase III studies. - Familiarity with producing and verifying analysis datasets (CDISC ADaM standard), and Tables, Listings and Figures. - Pinnacle 21 experience is strongly preferred. - Expert knowledge of SAS. - Professional leadership skills coupled with exceptional communication skills. 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 »
thinking in analysis of data. Excellent written and verbal communication. Experience with clinical databases, understanding of database structures, programming languages, datastandards (CDASH/CDISC) and application of these to CRF design, data handling and reporting. Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory 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 »
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 »
