ClinChoice

Senior/Principal Statistical Programmer Consultant-ONCOLOGY-REMOTE@EMEA

ClinChoice

Posted: a month ago
Senior Information Technology Full Time Completely Remote

Description Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds. ClinChoice is searching for a Senior/Principal Statistical Programmer Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

Responsibilities

  • Responsible for supporting the Programming deliveries of a clinical study or project.
  • Implements statistical programming aspects of the protocol and the clinical development program.
  • Ensures high quality is built into own deliverables and the quality delivered by other programmers.
  • Programs independently with high efficiency and quality.
  • Writes and/or implements specifications and oversees completeness of relevant documentation.
  • Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function.
  • Ensures compliance with standards and automation usage.
  • Plans and support team activities and tasks.
  • Communicates and escalates risks within the assigned studies and/or projects.
  • Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.

Requirements

  • Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience.
  • Need to have Oncology TA experience.
  • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
  • Good understanding of the clinical drug development process.
  • Strong communication skills and coordination skills.
  • Current knowledge of technical and regulatory requirements relevant for the role.
  • Ability to proactively manage concurrent activities within a project.
  • Proficient ability to influence relevant stakeholders on programming-related items.

About the Company ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

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