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Associate Director, Pharmacology Statistician

Date: Nov 23, 2020

Location: West Chester, Pennsylvania, US, 19380

Company: Teva Pharmaceuticals

Company Info
Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
Job Description

 

Reporting into the Head of Clinical Pharmacology Statistics in the Specialty Clinical Development group of Teva, as the Associate Director, Pharmacology Statistician would be part of the team who is responsible for providing statistical leadership for overall program and individual study strategy.  This role will allow you to demonstrate your leadership qualities, be creative and think strategically, all while playing a vital role with your knowledge of cutting-edge clinical trial design and methodology.  

 

By participating in First in Human (FIH)/clinical pharmacology studies, supporting Teva’s global regulatory submissions, you will be responsible for the statistical aspects of the design, implementation and analysis.  Working across multi-functional areas across the organization, you will determine the necessity and type of research that is required by providing strategic study design input and consultation for protocols.  You will also have the ability to communicate results to your respected audiences. 

 

You’ll also be responsible for:

  • Conduct modeling and simulation independently, or in collaboration with Pharmacometrics, Translational Sciences, DMPK teams to assist drug development strategies  
  • Leading the efforts to select CROs for outsourcing of statistical activities 
  • Collaborate with outsourcing partners and oversees conduct of statistical aspects of outsourced studies
  • Make decisions regarding work processes or operational plans and schedules in order to achieve department objectives
  • Consult, mentor, and teach other statisticians on statistical methodology, trial design, and data analysis
Qualifications

 

Required Qualifications:

  • Master's degree in Statistics, Biostatistics or related field of study with 10+ years of experience in Clinical statistics
  • PhD in Statistics, Biostatistics or related field of study with 6+ years of experience in Clinical statistics

 

Preferred Qualifications:

  • Experience in Clinical Pharmacology / FIH trials
  • Experience with modeling and simulation, multiple comparisons, missing data analysis, Bayesian methods in addition to knowledge of fundamentals in statistics
  • Experience with clinical development process, model informed drug discovery and development (MID3)
Function
Research & Development
Sub Function
Biometrics
Reports To

Director, Head of Clinical Pharmacology Statistics

Already Working @TEVA?

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Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.


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