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Job type: Permanent

Discipline: Statistics

Location: United Kingdom

A specialist contract research organisation (CRO) are looking to hire multiple Senior Programmers to work out of their UK offices. The organisation provides high quality analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas for the pharmaceutical industry. This position offers the exciting opportunity to work with a leading establishment and provider of real expertise in the biometrics field. You would be joining a team that is looking to invest in long term careers, focusing on quality of service, with up to date, relevant industry training.

Job Responsibilities:

Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, and CSRs.
Author and review simple and complex study TFL shells.
Author and review simple and complex dataset standards.
Perform data checks and data exploration (e.g. using frequencies, histograms).
Program, QC routine, and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice.
Complete and review CDISC Validation tool reports.
Ensure the appropriate standards are being applied and adhered to.
Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival).
Review project management related documents.
Maintain study master file documents and any other documents that are required to be audit ready.
Lead internal and client study team meetings effectively.
Present study updates internally and at client meetings.
Share scientific, technical, and practical knowledge within the team and with colleagues.
Perform work in full compliance with applicable internal and client policies, procedures, processes, and training.
Build effective collaborative working relationships with internal and client team members.
Seek opportunities to develop innovative ideas, sharing when appropriate.
Line manage or mentor more junior team members.
Contribute to the development of internal training materials.
Contribute to internal process improvement initiatives.

Skills and Requirements:

BSc, MSc, or PhD in numerical discipline (or relevant equivalent industry experience).
At least 3 years of relevant industry experience.
Understanding of clinical drug development process, relevant disease areas, endpoints, and study designs.
Awareness of industry and project standards & ICH guidelines.
Proficiency in data handling using SAS or other statistical software (e.g. R).
Demonstrable multitasking, project management, and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.

Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please Emma Adams at +44 203 854 3893 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

Proclinical Staffing is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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