Lead Statistical Programmer Consultant for Hematology Clinical Trials

3 weeks ago

Toronto, Ontario, Canada ClinChoice Full time
Job Title: Principal Statistical Programmer Consultant

ClinChoice is seeking a highly skilled Principal Statistical Programmer Consultant to join our team in the Hematology department. As a key member of our team, you will be responsible for leading and supporting all programming activities for clinical studies and regulatory submissions.

Main Responsibilities:
  • Develop and implement programming strategies to support clinical studies and regulatory submissions.
  • Lead and support programming teams to ensure timely and high-quality deliverables.
  • Collaborate with biostatisticians to customize outputs and graphics according to delivery specifications.
  • Ensure compliance with industry standards and automation usage.
  • Communicate and escalate risks within assigned studies and/or projects.
Requirements:
  • Bachelor's degree in computer science, statistics, or related scientific disciplines with 8 years of clinical programming experience.
  • Master's degree in CS, statistics, or related disciplines with 7 years of clinical programming experience.
  • Oncology/Hematology TA experience is required.
  • ISS & ISE experience is required.
  • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
About ClinChoice:

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. We are committed to inclusive, barrier-free recruitment and selection processes and are proud to be an equal opportunity employer.

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