Afternoon All Stat

 

Please see below details of an opportunity for a Principal Statistician/Manager in Surrey.  If you or someone in your network is seeking career development or a new location for the New Year, please get in contact.  For a confidential consultation call Alison Burton on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]

 

 

One of the world’s leading pharmaceutical companies is looking for a Principal Statistician/Manager to provide scientific statistical support & advice, working closely with Clinical, Medical and Data Operations team members.  In this role you will represent Biostatistics on project teams, coordinates Biostatistics project related activities and develop plans and timelines for the statistical activity on delegated projects.  A truly global organisation, they have an extensive and impressive track record of being at the forefront of innovative drug development and are in Top 10 pharmaceutical companies in the World.

 

Requirements;

 

• Provide scientific statistical input to development plans and to project planning as needed.

• Provide study design recommendations and prepare sample size calculations for Outline Protocols.

• Prepare statistical section for Clinical Study Protocols.

• Generate randomization schedules for clinical trials in accordance with protocols and maintaining security of schedules before and during the studies.

• Review Clinical Protocols.

• Provide input to the design of Case Report Forms and review discrepancy/edit check specifications and approve Case Report Forms

• Prepare Statistical Analysis Plans.

• Interact with Statistical programmers regarding programming requirements for analysis and reporting.

• Perform and Validate/QC statistical analysis.

• Prepare the statistical section of Topline and Final Clinical Study Reports.

• Review Final Study Reports.

• Present and discuss results with internal/external bodies as required.

• Lead project team meetings as needed.

• Generate and maintain study documentation.

• Attend and participate in project team meetings

 

Qualifications;

 

-Ideally, a PhD in Statistics or MSc or BSc degree and significant relevant experience.
- Extensive experience within either the pharmaceutical or consumer healthcare industry working with study teams to design, analyse and
  report clinical trials.
- Demonstrated experience of leading a therapeutic area.
- Ability to manage projects effectively to ensure timely execution.
- Ability to translate complex information in a compelling way to engage key stakeholders

 

For a confidential consultation call Alison Burton on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]

 

Alison Burton
Delivery Consultant – SEC Pharma

Statistics, Biostatistics & Programming
Tel: +44 (0) 207 255 6665
[log in to unmask]

 

Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician

 

 

 

 

 

 

 


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