Senior Statistical Programmer/Analyst Consultant (Oncology- Remote at UK-Outside

## About the Role As a Senior Statistical Programmer/Analyst Consultant at ClinChoice, you will be working directly with a single sponsor to deliver high-quality programming services for clinical trials. This is a unique opportunity to work with a global CRO, leveraging your technical skills and industry knowledge to drive programming efforts. You will be part of a talented team, collaborating with cross-functional stakeholders, including statisticians, data managers, and study leaders.

Your day-to-day responsibilities will involve leading and supporting programming tasks, ensuring compliance with regulatory requirements, and contributing to the development of best practices. You will have the opportunity to work on a variety of projects, including clinical studies and trials, and will be responsible for implementing statistical programming aspects of protocols and clinical development programs.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a senior statistical programmer, you will have the opportunity to work with a talented team, receive ongoing training and development, and contribute to the company's mission of accelerating the development and commercialization of innovative treatments.

## What You Will Do - Lead and support programming efforts for clinical trials, including data management and statistical analysis - Implement statistical programming aspects of protocols and clinical development programs - Collaborate with cross-functional teams, including statisticians, data managers, and study leaders - Ensure compliance with regulatory requirements, including ICH and Good Clinical Practices - Contribute to the development of best practices and standards for programming services - Write and implement specifications for programming tasks and oversee completeness of relevant documentation - Plan and support team activities and tasks, including resource allocation and timeline management - Communicate and escalate risks within assigned studies and/or projects - Work proactively with study team members to ensure high-quality deliverables - Develop and maintain relationships with key stakeholders, including sponsors and CRO partners

## What We Are Looking For - Bachelor's degree in computer science, statistics, or related scientific disciplines - At least 5 years of clinical programming experience, including CDISC standards and clinical trial process - Strong understanding of regulatory requirements, including ICH and Good Clinical Practices - Proficiency in programming languages, such as SAS or R - Experience working with clinical trials and studies, including data management and statistical analysis - Strong communication and coordination skills, with ability to work collaboratively with cross-functional teams - Ability to proactively manage concurrent activities within a project - Strong understanding of clinical drug development process and regulatory requirements

## Nice to Have - Master's degree in computer science, statistics, or related scientific disciplines - Experience working with oncology clinical trials and studies - Certification in clinical programming or related field - Proficiency in additional programming languages, such as Python or SQL

## Benefits and Perks - Competitive salary and benefits package - Opportunity to work with a global CRO, collaborating with talented teams and contributing to innovative projects - Ongoing training and development, including professional certification and education assistance - Flexible work arrangements, including remote work options - Access to cutting-edge technologies and tools, including statistical software and programming languages - Collaborative and supportive work environment, with opportunities for growth and advancement

- Highlight your experience with CDISC standards and clinical trial process, and be prepared to provide specific examples of your programming skills and expertise.

• Develop a strong understanding of regulatory requirements, including ICH and Good Clinical Practices, and be prepared to discuss your experience with compliance and quality assurance.
• Build a portfolio of your work, including examples of programming projects and collaborative efforts, to demonstrate your skills and expertise to potential employers.
• Prepare for interviews by researching the company and practicing your responses to common questions, such as those related to programming languages, clinical trials, and regulatory requirements.
• Consider pursuing certification in clinical programming or related field to demonstrate your expertise and commitment to the field.
• Be prepared to negotiate salary and benefits, and consider factors such as flexible work arrangements and professional development opportunities when evaluating job offers.