Senior Biostatistician

Warman O’Brien

  • Bruxelles
  • CDI
  • Temps-plein
  • Il y a 4 mois
Job Description

Our client is looking for a Senior Biostatistician (office based, with the possibility to be home based 3 days per week) to join their experienced and expanding team. They are a leading, global pharmaceutical with an exciting pipeline across a number of therapeutic areas including immunology and neurology.

The role is a Lead Biostatistician role responsible for one or more individual clinical studies within a clinical program or across multiple clinical programs. You will be required to provide statistical input to clinical studies, including input into the study design through statistical analysis and reporting.

Location:

Office based with the option of being home-based 3 days per week.

They offer:
  • Competitive salary
  • Flexible working options
  • Very competitive benefits package
  • Excellent career development opportunities
Role Responsibilities:
  • Acts as the lead biostatistician for one or more clinical studies within a clinical program or across multiple clinical programs.
  • Works very closely with the other biostatisticians and the program-level biostatistician and the lead biostatistician at the assigned CRO or other vendor.
  • Participates in the protocol summary development. Gives input into the study design, efficacy and safety parameters and the planned statistical analyses .
  • Authors the Statistical Analysis Plan (SAP) or reviews and approves the SAP if prepared by an external partner biostatistician.
  • Coordinates with other internal or external biostatisticians and statistical programmers to prepare the statistical analyses. Communicates and coordinates all statistical activities with external partner biostatisticians.
  • Reviews the clinical study report and provides input on interpretation of results by attending the Results Interpretation Meeting (RIM).
  • Assists the biostatistician lead for a program of studies with the statistical deliverables for regulatory submissions and the lifecycle of a development compound.
Person Specification:
  • Excellent understanding of SAS computing package.
  • Able to manage multiple tasks and projects.
  • Advanced statistical analysis skills.
  • Good clinical studies design and analysis experience.
  • Demonstrated experience in leading and participating in collaborative work teams at local and global levels, preferably including CROs.

Warman O’Brien