
Senior Clinical Data Scientist
15 hours ago
Job Overview
We are seeking a highly skilled Statistical Programmer to lead statistical programming support for multiple clinical projects using SAS. The ideal candidate will have extensive experience in developing statistical programming development with SAS and providing expert consultation across the organization.
Main Responsibilities
- Provide lead statistical programming support for multiple clinical research study projects or study teams, ensuring timely and accurate delivery of high-quality results.
- Develop and implement sound methodologies for clinical trials research involving CDISC standards and analysis data sets, demonstrating expertise in programming techniques and regulatory requirements.
- Collaborate with cross-functional teams to develop and review programming documentation, annotations, and specifications, adhering to relevant Standard Operating Procedures.
- Conduct code reviews, write well-documented, efficient, and high-quality code, and support programming validation as needed.
Qualifications and Skills
- A bachelor's degree plus 4 years of experience in statistical programming, preferably in a Pharmaceutical/CRO environment, with a strong understanding of CDISC/TLF standards.
- Familiarity with GCP principles and other regulatory standards in Clinical Research, including knowledge of E-submissions and study requirements.
- Excellent analytical skills, with the ability to process scientific and medical data, and communicate complex information effectively.
Benefits of Joining Our Team
- Opportunities for professional growth and development, with a focus on continuous learning and skill enhancement.
- A collaborative and dynamic work environment, with a team of experienced professionals dedicated to delivering high-quality results.
- Competitive compensation and benefits package, designed to attract and retain top talent in the industry.
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