Senior SAS Programmer required
We are currently working with a reputable innovative Global Pharmaceutical company who are now looking for a Senior Statistical Programmer (SAS). This exciting opportunity will be responsible and accountable for the programming aspects of all clinical studies or project(s) conducted, and responsible for effective communication within the corporation and, where appropriate, with external organisations of the issues and actions related to the successful completion of programming activities within the project(s).
ü Hybrid working from Central London - 3 days per week
ü Competitive salary with bonus and benefits
ü Commuting costs will be reimbursed
Key Accountabilities;
· Keep in accordance with the Quality Management System, working practices, Good Clinical Practice, and ICH, ensuring that training in these areas is always kept up to date.
· To ensure that all programming responsibilities follow Good Programming Practice (GPP).
· Responsible and accountable for all programming aspects of a clinical study and where appropriate the development project(s).
· Primary UK contact for all programming activities of the study or project(s).
· Primary contact for external consultants and Service Providers (SPs) for all appropriate programming activities of the study/project(s).
· Contributing to and be accountable for the setting up, implementation and reporting of clinical study(s) within all appropriate programming aspects of the study(s) as the programming lead for the study/project(s).
· Acting as an advisor to the UK clinical/research scientists engaged in the scientific aspects of the clinical development study/project(s) and providing programming support to UK clinical scientists engaged in the study/project(s).
· Contributing to the development and maintenance of policies, SOPs and UK documents.
· Ensuring learning and knowledge transfer during and at the completion of the project.
· Continue to update knowledge and keep abreast of changes within the field of Programming in Clinical Development
Experience required;
· Relevant, in depth and demonstrated experience within the pharmaceutical, contract research organisation (CRO), biotechnology or medical sector, including programming of SDTMs, ADaMs, macro creation, Tables, figures and listings development and reporting.
· Demonstrated proficiency with ICH/GCP guidelines, related programming guidelines (GPP) and knowledge of other regulatory guidelines relating to statistics.
· Flexibility and the ability to manage multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
· Ability to oversee and manage CROs conducting programming aspects of clinical trials and to ensure high quality deliverables are received.
· Able to interact effectively at all levels within the organisation, as well as with external partners and clients.
· Minimum BSc in Mathematics, Statistics, or Computing or related discipline, or equivalent combination of education and experience.
If this roles sounds of interest please apply direct, send your CV to julie.ball@cpl.com or call 0118 995 2143 for a further conversation
- Agency: Cpl Life Sciences
- Reference: JO-2308-521980
Website: Cpl Life Sciences
- Posted: 5th September 2023
- Expires: 3rd October 2023
