Job Overview :
Senior Statistical Programmer required to work for Labcorp Drug Development on early phase healthy volunteer studies
Multiple Sponsors, multiple therapy areas
Excellent opportunities to progress
Varied, fast paced environment
Office based in any European or South African offices or work from home anywhere in Europe or South Africa
Candidates must have experience of working as a Lead Statistical Programmer within a healthcare company within Europe or South Africa
Join our growing team in 2022 and discover your extraordinary potential by working as a Labcorp Drug Development Senior Statistical Programmer within our Early Phase statistical programming department.
As a Senior Statistical Programmer at Labcorp Drug Development you will assume the role of Lead Programmer for allocated studies, developing and maintaining SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs.
Working within early phase statistical programming we offer, in a word, variety
In the type of studies : PK, Bioequivalence, Metabolism, Dose Escalation etc. and Sponsors
In Early Phase we are not assigned for years to the same study, so you will be exposed to multiple studies for clients with different needs as well as working with talented internal colleagues
Job Primary Functions
Perform the role of the Lead Statistical Programmer.Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
Develop and maintain SAS programs to create complete SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs
Produce Define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
Develop and / or lead the development of complex specifications for SDTMs and ADaM datasets and contribute to the development of Covance and Client standards
Review SAPs and TFL shells from a programming perspective for studies and advise on the development of complex TFL shells from a programming perspective
Mentor less-experience programmers in the processes around SDTMs, ADaMs and TFLs ensuring adherence to department practices and processes
Present and share knowledge at department meetings
Respond to QA and client audits and support qualification audits
Contribute to proposal activities and participate in bid defenses meetings in order to win new business
Continually identify and suggest ways to improve the efficiency, quality and productivity of statistical programming
Education / Qualifications :
BSc, preferably in computing, life science, mathematical or statistical subject
Experience :
Candidates must have experience of working as a Lead Statistical Programmer within a healthcare company
Show evidence of and experience of leading studies and experience in study set-up and review of study specific documents
Knowledge of CDISC requirements
Positive attitude and willingness to learn and contribute in a team setting and communicate effectively within the team environment
Good organization skills and the ability to prioritize own work
Self motivation and ability to work independently
A cooperative and team-oriented approach
You must be fluent in English language (both verbal and written)
If you're looking for a role in a fast-paced environment leading multiple studies for key clients, then Labcorp Drug Development is the place for you!
NO AGENCIES PLEASE
MORE INFORMATION AVAILABLE ON REQUEST
For a confidential discussion about this opportunity, please phone Peter Lewis on +44 (0) 7917 710 602 or you can text me via WhatsApp on the same number.
To apply, please click on the APPLY button.
Keywords :
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