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Associate Director, Statistical Programming

Tyra Biosciences · Remote, US · Remote

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About Tyra Biosciences

Backed by Canaan Partners.

About the role

Lead statistical programming activities for multiple clinical studies and development programs from study startup through study closeout and regulatory submission. Accountable for the quality, accuracy, timeliness, and completeness of all statistical programming deliverables across assigned studies and programs. Found on 1752vc Careers, the job board for startup and VC roles.

What they're looking for

  • Bachelor's degree in Statistics, Mathematics, Computer Science, or related discipline with 8-10+ years of statistical programming experience in biotech, pharmaceutical, or CRO environments, or Master's degree with 6-8+ years of relevant experience
  • Demonstrated experience leading statistical programming activities across multiple concurrent clinical studies and development programs
  • Software Knowledge: A comprehensive knowledge of SAS and CDISC standards. Strong knowledge and skills of programming in SAS
  • Pinnace 21 knowledge for validation and submission
  • Ability to meet deadlines and perform multiple tasks in a fast-paced setting. Prior experience working in a small, start-up biotech work environment preferred
  • Excellent written and oral communication skills
More about this role

Tyra Biosciences, Inc. is seeking a highly motivated Associate Director, Statistical Programming, to make impactful contributions to projects targeting disease areas with high unmet medical needs. The successful candidate will be highly organized, self-motivated, and thrive in a dynamic, cross-functional start-up environment.

This position will support multiple clinical studies and be accountable for the timely delivery, quality, and integrity of statistical programming deliverables. The role will also contribute to the development, standardization, and continuous improvement of the Statistical Programming infrastructure, processes, and tools.

Lead statistical programming activities for multiple clinical studies and development programs from study startup through study closeout and regulatory submission.

Accountable for the quality, accuracy, timeliness, and completeness of all statistical programming deliverables across assigned studies and programs.

Perform hands-on statistical programming activities as needed, including development and validation of SDTM, ADaM, TLFs, and exploratory analyses

Provide technical oversight and review of programming deliverables generated by...

Read the full posting on Tyra Biosciences's site ↗

Data Science & Biometrics

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