Senior Statistical Programmer/Analyst Consultant--(Oncology)

About the role

This is a client-facing, delivery-focused role that works under the leadership of a Programming team leader to lead and/or support the programming effort for a clinical study or project. You will collaborate with study team members including Statisticians, Lead Programmers, Data Managers, and Study Leaders while ensuring high-quality, compliant deliverables.

Responsibilities

• Support the Programming deliveries of a clinical study or project.
• Implement statistical programming aspects of the protocol and the clinical development program.
• Ensure high quality is built into your own deliverables and those of other programmers.
• Program independently with high efficiency and quality.
• Write and/or implement specifications and oversee completeness of relevant documentation.
• Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function.
• Ensure compliance with standards and automation usage.
• Plan and support team activities and tasks.
• Communicate and escalate risks within the assigned studies and/or projects.
• Work proactively with cross-functional study team members.

Requirements

• Bachelor’s degree in computer science, statistics, or related scientific disciplines with 5 years of clinical programming (CDISC) experience; OR Master’s degree in computer science, statistics, or related disciplines with 6 years of clinical programming (CDISC) experience.
• Oncology therapeutic area experience.
• Working knowledge of ICH and Good Clinical Practices, clinical research, the clinical trial process, and related regulatory requirements and terminology.
• Good understanding of the clinical drug development process.
• Strong communication 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 ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of proven high-quality delivery, ClinChoice employs over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our mission is to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. We prioritize employee development, offering continuous training to maintain highly-qualified personnel and below-industry-average turnover rates. ClinChoice is an equal opportunity employer committed to diversity and inclusivity.