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Job Details

Principal Statistician ~ Top-Pharma

Company: RBW Consulting
Location: Mid-West, USA (full relocation offered)
Reference: DWC-PRINC-STATPHARM
Closing Date: 22 Dec 16
Type: Full Time
Salary (£): Competitive
Benefits: $excellent, with a strong accompanying package

Job Summary:

After a number of very positive results in a Phase III trial, a top-Pharma looks to further bolster its Biostatistics team.

Requirements:

Role

  • Serve as statistical lead of on assigned projects
  • Represent organisation in all correspondence with regulatory authorities globally
  • Oversee and manage 3rd parties where necessary (CROs, etc.)
  • Represent statistics in cross-functional meetings
  • Input into the design of clinical trial protocols, suggesting best statistical design, acceptable by regulators
  • Lead the preparation of statistical analysis plans, working with statistical programmers to create the mock table shells
  • Analyse clinical trial data
  • Lead the statistical contribution to the Clinical Study Report and other documentation associated with submission activities
  • Mentor and support junior statistics staff
  • Proactively participate in departmental process improvement

 

Qualifications

  • MSc or PhD in relevant discipline
  • Robust industry experience
  • Excellent experience of project management in a clinical trials setting
  • Well-versed in SAS programming
  • Very strong communications skills – written and verbal

 

I manage a range of other permanent and freelance positions for a broad portfolio of clients (Biotech, CRO and Pharma). If the above role isn’t for you but you’d nevertheless like to discuss your options in the market, I’d welcome a confidential discussion by phone or email. Contact Daniel Cheetham at (646) 586 9087.

 

Keywords
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Apply for this job: Principal Statistician ~ Top-Pharma

Contact Information:

Address:  Brighton
Southdown House, 130a Western Road, Brighton BN1 2LA
BN1 2LA
England
Tel:  01293 584 300

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