Senior Statistical Programmer
Salary Range: 120,000-$150,000
My client is a pioneering biotechnology firm at the forefront of innovation in the CNS/Neurodegenerative space. They are looking to bring on a Principal Statistical Programming consultant with a strong background working on stage 2 and 3 Neurological studies. The company is led by highly experienced drug developers, scientists and visionaries all collaborating to develop breakthrough therapies aimed to slow the progression of Huntington disease. They currently have a product in late-stage clinical development for ALS and Huntington Disease, and two other studies entering phase 2. They are close to submitting an NDA, so now is a perfect time to get in a capitalize on their growth!
The successful candidate will be instrumental in the execution of statistical programming tasks, supporting the analysis and interpretation of data from clinical trials and research studies.
Responsibilities:
- Statistical Programming:
- Develop, validate, and maintain statistical programs for the analysis and reporting of clinical trial data, ensuring accuracy and compliance with regulatory standards.
- Collaborate with cross-functional teams, including statisticians, data managers, and clinical researchers, to understand project requirements and deliver high-quality programming solutions.
- Data Analysis Support:
- Assist in the production of statistical outputs, tables, figures, and listings to support data analysis and interpretation.
- Contribute to the development and implementation of data visualization techniques to enhance data presentation and understanding.
- Quality Assurance:
- Conduct thorough reviews and validation of statistical output to ensure data integrity, reliability, and adherence to internal and external standards.
- Implement and maintain quality control processes to uphold the highest standards in statistical programming deliverables.
- Documentation:
- Generate and maintain comprehensive documentation, including programming specifications, validation plans, and other relevant documentation.
- Ensure that all programming activities adhere to company SOPs, regulatory guidelines, and industry best practices.
- Collaboration and Communication:
- Collaborate effectively with cross-functional teams, providing programming expertise and support for study-related activities.
- Communicate results and findings clearly to team members, fostering a collaborative and transparent work environment.
Qualifications:
- Bachelor's, Master's, or Ph.D. in Statistics, Biostatistics, Computer Science, or a related field.
- 7-10 years of experience in statistical programming, preferably in a biotechnology or pharmaceutical setting.
- Proficiency in programming languages such as SAS and/or R.
- Solid understanding of clinical trial processes, data standards, and regulatory requirements.
- Strong attention to detail, problem-solving skills, and the ability to work independently and collaboratively.
