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Biostatistician II - Non-clinical

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

PhD or Master in Statistics, 5-8 years of relevant experience, Experience in bioanalytical pharmacokinetic studies, None.

Key responsabilities:

  • Contribute to statistical strategies for studies
  • Lead production and quality control of reports

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Parexel XLarge http://www.parexel.com
10001 Employees
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

  • PhD or Master in Statistics or related discipline with relevant experience of 5 - 8 Years.
  • Expericence in bioanalytical & pharmacokinetic studies.
  • Contributes to statistical strategies for nonclinical and clinical bioanalytical assay development , GLP and non-GLP drug safety studies like study design , protocol development , SAP, trial design, protocol and CRF development on specific studies.
  • Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.
  • Perform sample-size calculations, generate randomization lists, and write statistical methodology sections for inclusion in study protocols

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Teamwork
  • Communication
  • Problem Solving

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