To assist the Head of Statistics in providing timely communication to the function; Leadership of members of the statistical function within specific geographical regions; Line manage senior members of staff within the statistics function, allowing individuals the opportunity to reach their full potential; Training and mentoring line managers and less experienced members of staff within the Statistics function; Support resolution of any issues escalated by or involving statistics team members; Support the operational success of studies through careful planning and work assignments; Helping the Head of Statistics identify areas of skill development for the statistics function as a whole; Work closely with cross-functional Operational leadership team
Requirements:
Educated to PhD or MSc in Biostatistics or a related discipline; Experience within the pharmaceutical industry to have a good awareness of clinical trial issues, design, and implementation; Familiarity with GCP and regulatory requirements; Experience of writing SAPs, protocols & regulatory submissions
Text:
Associate Director, Statistics To assist the Head of Statistics in providing timely communication to the function; Leadership of members of the statistical function within specific geographical regions; Line manage senior members of staff within the statistics function, allowing individuals the opportunity to reach their full potential; Training and mentoring line managers and less experienced members of staff within the Statistics function; Support resolution of any issues escalated by or involving statistics team members; Support the operational success of studies through careful planning and work assignments; Helping the Head of Statistics identify areas of skill development for the statistics function as a whole; Work closely with cross-functional Operational leadership team Educated to PhD or MSc in Biostatistics or a related discipline; Experience within the pharmaceutical industry to have a good awareness of clinical trial issues, design, and implementation; Familiarity with GCP and regulatory requirements; Experience of writing SAPs, protocols & regulatory submissions
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