Statistical Programmer
Responsibilities:
- You will work within the Scientific Programming team to provide support to the analysis and management of our clinical trials and have the opportunity to significantly contribute to special projects that will revolutionize some of our keyways of working.
- Develop and maintain reporting solutions in the context of Translational and Clinical R&D.
- Design visualizations that give clear and accurate insights to end users.
- Develop data visualization to support primary and exploratory analysis of clinical trial data.
- Gather requirements from target end users and translate their business problems into technical solution.
- Evaluate existing standard programs to identify opportunities to simplify, add flexibility, or otherwise improve them, as well as research and evaluate methods to optimize program performance.
- Participate in transitioning statistical programming from a SAS-based to R-based platform.
Requirements:
- Minimum of one year of work experience co-relating to the position's responsibilities.
- Understanding of clinical and research data.
- Demonstrated growth mindset that includes embracing change, learning from mistakes and challenges, innovating, motivation, and teamwork in a global team.
- Curious, analytical, proactive team member who seeks opportunities to learn and contribute.
- Enjoy playing with data to extract scientific evidence.
- Master's Degree in Life Sciences.
- Effective oral and written communication skills in an English global environment and ability to have efficient exchanges with partners and colleagues across geographic locations.