ProClinical is excited to announce that an exciting opportunity has arisen for a Statistical Analyst to join a scientifically driven, global, full-
service clinical contract research organisation (CRO). The company accelerates the global development of safe and effective medical therapeutics through its high-
science and disciplined operating approach across all major areas including oncology, cardiology, and metabolic diseases.
The Statistical Analyst will be stationed with the company's team in London.
Job Responsibilities :
Writing statistical programs for use in creating analysis datasets, tables, listings, and figures according to specifications.
Reviewing analysis plans for appropriate methods.
Programming study analyses and reviewing study results.
Communicating the project requirements for cleanup and data capture to ensure the key study variables are suitable for analysis.
Skills and Requirements :
A Masters' degree.
Demonstrable industry working experience with SAS programming or SAS certificates.
Proven knowledge of databases and data management processes.
Proven knowledge of statistical methods commonly used in pharmaceutical clinical trials.
Proven knowledge of CDISC standard databases (SDTM and ADaM) and data management processes.
Excellent organisational and communication skills.
Strong interpersonal skills, with an ability to interact cross-functionally and at all levels of the organisation.
Excellent written, verbal communication, and presentation skills.