6 month rolling contract
UK based – M4 Corridor
For a confidential consultation call Priya Mukherjee on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]
Summary:
Participates in business development and client liaison as required.
Provides technical leadership within the SAS programming team including line management as required.
Ensures clinical trials are conducted such that subjects’ rights, safety and wellbeing are protected and that the clinical trial data are reliable.
Ensures the client fulfils its obligation to provide clients with appropriate strategic and technical advice for statistical programming related elements of their clinical development programmes.
Acts as point of contact for both internal and external customers for all statistical programming issues for allocated studies.
Maintains up to date knowledge of relevant regulatory guidance and requirements.
Essential Skills:
Proven relevant programming experience within the pharmaceutical industry or clinical research organisation.
Experience in the production and QC of datasets, tables, figures and listings to summarise and analyse clinical data using SAS.
Comprehensive knowledge of the clinical development process and its critical paths.
Experience of leading multiple studies concurrently.
Awareness of global regulatory environment.
Excellent knowledge of ICH-GCP.
Experience of a wide breadth of therapeutic areas.
Experience of working in multi-disciplinary teams.
Experience of line management and training of other colleagues.
Significant experience of representing statistical programming at face to face meetings with clients.
Good knowledge of statistical programming process metrics and budgets.
Rates on offer are excellent and negotiable, and can be discussed upon application.
Best wishes,
Priya
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