About this role
The team is seeking a Senior Statistical Programmer to join their team, dedicated to one of their global pharmaceutical clients. In this role, you will be fully embedded within the team organization, contributing to innovative patient treatment solutions. You will have the opportunity to work autonomously while receiving support from the team, making this an exciting time to be involved in a new program.
Key Responsibilities:
- Develop and validate statistical programs for clinical trial data analysis.
- Collaborate with biostatisticians and clinical teams to ensure accurate data interpretation.
- Prepare and review statistical analysis plans and programming specifications.
- Ensure compliance with regulatory standards and guidelines.
- Mentor junior programmers and provide guidance on best practices.
- Participate in project meetings and contribute to strategic discussions.
Required Skills & Qualifications:
- Proficiency in statistical programming languages such as SAS or R.
- Strong understanding of clinical trial processes and regulatory requirements.
- Experience with data management and statistical analysis techniques.
- Excellent problem-solving skills and attention to detail.
- Ability to work independently as well as part of a team.
Experience:
- Minimum of 5 to 8 years of experience in statistical programming, preferably within the pharmaceutical industry.
What we offer:
- A dynamic work environment with opportunities for professional growth.
- The chance to work on cutting-edge projects that impact patient care.
- Supportive team culture that values autonomy and innovation.
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.