About this role
As a Senior Statistical Programmer, you will be fully embedded within one of our global pharmaceutical clients, playing a crucial role in the development of innovative patient treatments. You will have the opportunity to work autonomously and take ownership of your projects, supported by the team throughout your journey.
Key Responsibilities:
- Develop and validate statistical programs for clinical trial data analysis.
- Collaborate with biostatisticians and clinical teams to ensure the integrity and accuracy of data.
- Create and maintain documentation for statistical programming processes and methodologies.
- Perform quality control of programming outputs and ensure compliance with regulatory standards.
- Contribute to the development of programming standards and best practices.
Required Skills & Qualifications:
- Proficiency in SAS and/or R for statistical programming.
- Strong understanding of clinical trial processes and regulatory requirements.
- Experience with CDISC standards, particularly ADaM and SDTM.
- Excellent problem-solving skills and attention to detail.
- Strong communication skills to effectively collaborate with cross-functional teams.
Experience:
- Minimum of 5-8 years of experience in statistical programming within the pharmaceutical or biotechnology industry.
What we offer:
- An opportunity to work on cutting-edge projects that impact patient treatment.
- A collaborative and supportive work environment.
- Opportunities for professional development and career advancement.
Applications are read by our talent team, usually within two working days.
If you look like a fit we will call you, and you will hear from us either way.