3 дня назад
Senior Statistical Programmer/Analyst Consultant (Oncology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Statistical Programmer/Analyst Consultant (Oncology) (Clinical Programming/CDISC): Delivering statistical programming for oncology clinical studies and development programs with an accent on protocol implementation, documentation, quality, and regulatory compliance. Focus on independently programming study deliverables, applying CDISC and automation standards, coordinating with statisticians and data managers, and escalating project risks.
Location: Remote within the United Kingdom; outside IR35 contract
Company
is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.
What you will do
- Support programming deliveries for oncology clinical studies and projects.
- Implement statistical programming aspects of protocols and clinical development programs.
- Program independently while maintaining high efficiency and quality across deliverables.
- Write or implement specifications and oversee the completeness of programming documentation.
- Apply standards and automation practices, contribute to process improvements, and support team activities.
- Coordinate with statisticians, lead programmers, data managers, study leaders, and other study team members while communicating and escalating risks.
Requirements
- Bachelor’s degree in computer science, statistics, or a related scientific discipline with 5 years of clinical programming experience, or a master’s degree with 6 years of experience.
- Clinical programming experience with CDISC is required.
- Oncology therapeutic-area experience is required.
- Working knowledge of ICH, Good Clinical Practice, clinical research, clinical trial processes, and regulatory requirements.
- Strong communication, coordination, stakeholder-influencing, and concurrent-activity management skills.
- Current knowledge of technical and regulatory requirements relevant to clinical programming.
Culture & Benefits
- Work directly with a single sponsor while receiving the support and career opportunities of a global CRO.
- Independent, client-facing work within a high-trust environment.
- Continuous training and professional development.
- International organization with more than 4,000 professionals across over 20 countries.
- Supportive, diverse, and inclusive work culture.
Hiring process
- Submit a CV and receive an acknowledgement of receipt.
- Selected candidates are invited to a phone interview as the first step.
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