
Senior Clinical Trials Programmer
1 day ago
We are dedicated to delivering innovative solutions that improve lives and make a lasting impact on the world.
Job RoleWe seek an experienced professional to join our team as a Study Designer and Edit Check Programmer. As a key member of our Clinical Systems and Analytical Reporting team, you will play a crucial role in building and programming studies in our clinical trial database.
Your responsibilities will include:
- Supporting clinical trial platform technologies
- Acting as a data scientist to bring awareness to patterns and analytical insights
- Coordinating and providing programming support to Clinical Study Teams
- Ensuring efficient and consistent use of EDC systems and compliance with established procedures or standards
- Good understanding of Good Clinical Practice
- Experience in data management, performance management techniques, problem-solving, and analytical thinking
- Familiarity with clinical trials processes, data management processes, and clinical trial databases
- Programming languages: Edit check development and Custom function programming
- Advanced degree in life science, computer science, math, statistics, business administration, or related discipline
- Broad knowledge and work experience in data management, programming in the Pharmaceutical or Biotech area
- General project management and planning experience
You are a strong leader who can confidently influence stakeholders and contribute individually to study-specific and general CSAR GDO projects or operational work.
What We OfferAs a member of our team, you will have the opportunity to work with a collaborative, innovative, and science-based culture that values teamwork and excellence.
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