Senior Statistical Programmer (UK Remote)

Recruiter
Cytel
Location
London (Greater)
Posted
18 Apr 2019
Closes
23 Apr 2019
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Summary of Job Responsibilities:

As member of the FSP or PBS (Project Based Services) departments, and reporting to the Global Head of Statistical Programming or to the local manager (Director statistical programming or Associate director of statistical programming), the main responsibilities of the Senior Statistical Programmer will be to:


Lead, or contribute to, statistical programming activities on BDM projects (development or QC of deliverables):

delivering exemplary performance and solving complex technical problems to inspire other programmers,
ensuring an efficient collaboration with BDM global teams (Europe, India, and US)
being accountable for the quality, traceability, reproducibility and timeliness of statistical programming deliverables,
being accountable for overall client satisfaction with these deliverables,
maintaining a detailed project and validation plan,
efficiently communicating with internal and external clients,
ensuring budget monitoring and adherence


Ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements, for instance:

Clinical study reporting, e.g. ICH E3
Electronic records handling, e.g. Chapter 21 of the US Code of Federal Regulation - Part 11
Electronic submission of clinical data to agencies, e.g. e-CTD guidance and CDISC SDTM and ADaM standards


Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g. biostatisticians, data managers, medical writers…)
Understand, follow and ensure adherence to all BDM SOP as well as any other relevant SOPs.
Keep abreast of current and new statistical programming techniques and other applicable technical advancements while assisting in their implementation
Occasionally, responsibilities will also include to:




When needed, interact with regulatory agencies regarding specifications for electronic submissions, and direct/develop statistical programming electronic submission deliverables Contribute to budget evaluation for proposal writing purpose.
Lead, or contribute to, the design of new statistical programming processes or optimization of existing ones to reach the best productivity, to ensure the best quality of the statistical outputs, and to reach the best customer satisfaction (internally and externally) with flexibility, reliability and responsiveness.
Qualifications and Experience:




Minimum Education: BSc or equivalent with research experience, and/or MS (in a numerate discipline preferably in Statistics, Computer Science, or Mathematics)



Minimum Work Requirements:



Preferably at least 5 years of experience in biostatistics or statistical programming activities in the Pharmaceutical/Biotechnology industry in clinical development
Experience as a lead statistical programmer on several concurrent projects
Proficient in SAS
Good knowledge of CDISC ADaM and SDTM.
Good understanding of drug development, including knowledge of interfaces and interdependencies with other functions.
Good knowledge of relevant regulatory and data submission guidelines.
Project management skills



Skills:



Fluent in English (French and/or German is a plus)
Ability to work effectively in international teams, effectively operates within a matrix organization and with multi-disciplinary groups, excellent team player with strong interpersonal skills contributing to building the team spirit
Ability to rapidly understand and anticipate the needs of internal and external customers, and respond to their inquiries
Good negotiation and issue resolution skills
Ability to educate internal and external interfaces (providers and customers) on the statistical programming processes, and the underlying regulatory requirements
Mentoring skills


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