ClinChoice

Principal Biostatistician Consultant

ClinChoice

contract

Posted on:

Location Type: Hybrid

Location: New Jersey • Pennsylvania • United States

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Job Level

Lead

About the role

  • Work with Biometrics director to manage one or more compounds/Indications in R&D for the entire life cycle.
  • Responsible for all statistical aspects of the drug development and/or post-approval programs.
  • Coordinate statistical and programming support and manage contractors/CROs when necessary.
  • Serve as lead statistician for clinical studies and collaborate effectively with the study team members.

Requirements

  • M.S. or Ph.D. (or equivalent) in Statistics or Biostatistics is required.
  • Minimum 4 years (Ph.D.) or 8 years (M.S.) pharmaceutical industry experience
  • Should possess experience interacting with regulatory agencies (e.g. FDA, MHRA or EMEA).
  • Experience managing multiple projects/therapeutic areas.
  • Experience in managing external vendors (e.g. contractors, CROs).
  • Capability in working independently and lead one or multiple clinical studies.
Benefits
  • Competitive salary
  • Hybrid work arrangement
  • Opportunities for professional development
  • Access to a supportive culture
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
statistical analysisdrug developmentclinical studiesbiostatisticsproject managementregulatory complianceprogramming supportdata analysisstatistical programming
Soft Skills
collaborationleadershipindependent workcommunicationorganizational skills
Certifications
M.S. in StatisticsPh.D. in Biostatistics