Cytel is seeking a highly experienced Senior or Principal Statistical Programmer to join our FSP Services team, working fully embedded within a global pharmaceutical client. You will play a pivotal role in driving the next generation of patient treatment by providing expert technical support and overseeing clinical development programs across various therapeutic areas.
Key responsibilities
- Implement all reporting and analysis activities for sponsor clinical trials with a high degree of autonomy.
- Provide expert technical guidance and mentorship to team members to ensure consistent, high-quality data deliverables.
- Oversee and coordinate with CRO programmers to maintain project timelines and data integrity.
- Work independently on complex clinical development programs with minimal supervision.
- Collaborate closely with the client's biostatistics and programming teams to support innovative research initiatives.
Requirements
- Extensive experience in statistical programming within the pharmaceutical or clinical research industry.
- Advanced proficiency in SAS and R programming languages for clinical data analysis.
- Proven ability to work independently and manage complex clinical development projects.
- Strong leadership skills with experience in overseeing external partners or CRO teams.
- Excellent communication skills and the ability to thrive in a fully remote, client-dedicated environment.
What we offer
- The opportunity to work with a global pharmaceutical leader while being supported by the expertise of Cytel.
- A fully remote work environment that empowers autonomy and professional ownership.
- Exposure to diverse therapeutic areas and cutting-edge clinical research programs.
- Professional growth within a specialized FSP Services business unit.