inVentiv Health -Transforming Promising Ideas into Commercial Reality
inVentiv Health Clinical is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 14,000 passionate employees supporting clients in more than 70 countries, inVentiv Health works to accelerate high quality drug development programs of all sizes around the world.
Here at inVentiv Health we are currently recruiting for the below Statistical roles:
Senior Statistical Programmer - Europe wide (permanent) – home based
• Dedicated to a specific FSP as part of a global Biometric team
• Responsible for performing all SAS programming tasks required to support the conduct, statistical analysis and reporting of projects, and acts as the lead statistical programmer on multiple projects.
• Significant experience with SAS programming in a relevant clinical trial environment is required
SAS Programmer – London, UK (6 months contract) – home/office
• Advanced knowledge of SAS, including statistical procedures, macros, and graphics
• Clinical trial experience in Pharmaceutical and/or Biotech companies and/or CRO’s
• Knowledge of CDISC requirements for SDTM and ADaM
• Ability to interpret statistical analysis plans and table shells to create analysis datasets and TLGs
• Knowledge of statistical methods in clinical study designs is an advantage, clinical data analyses (from Phase I through Phase IV).
Biostatistician – South of UK (permanent) – home based
• Will work closely and be solely dedicated to a specific FSP as part of a global Biometrics team.
• Responsible for managing and leading assignments on single or multiple Phase IIIb-IV Observational projects
• Previous experience working on Observational studies required
• Can consider candidates with Statistical Programming background looking to move into a Biostatistician role
Senior SAS Programmer – UK (permanent) – home based
• Provide statistical programming support for assigned project
• Develop general SAS application code
• Validate SAS programs and analysis results
• Assists in Quality Control activities
Senior Statistician – UK (permanent) – home based
• Submissions experience to the FDA or regulatory body
• Prepare statistical section for Clinical Study Protocols
• Provide input to the design of Case Report Forms and review Edit Check Specifications
• Preparation of Statistical Analysis Plans.
If you have the required experience for any of these positions and are eligible to work in the UK (or Europe when based EU wide) then please apply by sending your CV to [log in to unmask] or contact Ellie Zavrelova on +44 (0) 1628 408 455.
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