Associate Director Biostatistics - 4401 | Warman O’Brien

Job Details

Associate Director Biostatistics

  • 195000
  • Nutley, New Jersey, United States
  • Permanent
We have partnered with a global, award-winning pharmaceutical company who are searching for a driven, highly analytical Associate Director Biostatistics to help support their Biostatistics department with end-to-end clinical study design, analysis, and publication. Working across a range of complex, ground-breaking projects, this position offers you the opportunity to become an integral part of a company striving to improve the practice of medicine worldwide.

What is it like to work here?
  • You will have the chance to work on several novel, innovative projects within neurology and oncology at one of the world’s leading pharmaceutical companies.
  • Experience for yourself what it’s like to work in a company that prides itself on its ethos for excellence.
  • Enjoy being part of a dynamic work environment where your voice is truly valued, and high performance is rewarded.

What will you be doing?
  • Offer your statistical support to optimise efficiency in the end-to-end design and implementation of clinical trial programs and research projects.
  • Use your expertise to lead multiple global trials and execute diverse statistical tasks.
  • You are expected to drive excellence from both project lead and, concurrently, team member perspectives – maintaining the highest quality standards whilst achieving timely deliverables.
  • Liaise with the relevant regulatory bodies and health authorities and offer statistical support in preparation of all regulatory documents.
  • Data analysis, interpretation, reporting, presentation, and publication support.
  • Statistical support for analysis datasets, tables, figures and listings.
  • Protocol review, CRF design, SAP writing, TLG shells, CSR writing and data management plan reviews.
  • Continual cross-collaboration with other study-related personnel including clinicians and CRO statisticians.

What do you bring to the table?
  • Master’s or PhD in biostatistics, statistics, mathematical analysis, or related degree.
  • Demonstrable Pharmaceutical industry experience.
  • Experience with FDA submissions.
  • Excellent communication skills.
  • Strong working knowledge of SAS or R.

What will you get in return?
  • Clear career progression and development pathways.
  • Competitive salary (dependent on experience).
  • Benefits – 20% bonus, 15k LTI  healthcare, 401K.
Robyn O'Toole Associate Recruitment Consultant

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