About this role
The team is seeking a Senior Statistical Programmer with expertise in SDTM (Study Data Tabulation Model) to join their dynamic team. This role involves working closely with biostatisticians and data managers to ensure the accurate and timely delivery of clinical trial data.
Key Responsibilities:
- Develop, validate, and maintain statistical programs for clinical trial data.
- Create SDTM datasets in accordance with regulatory guidelines and industry standards.
- Collaborate with cross-functional teams to ensure data integrity and compliance.
- Perform quality control checks and troubleshoot programming issues as they arise.
- Contribute to the preparation of statistical analysis plans and reports.
Required Skills & Qualifications:
- Proficiency in SAS programming and experience with CDISC standards, particularly SDTM.
- Strong understanding of clinical trial processes and data management.
- Excellent analytical and problem-solving skills.
- Ability to work independently and as part of a team in a fast-paced environment.
- Strong communication skills, both written and verbal.
Experience:
- 5-8 years of relevant experience in statistical programming within the clinical research industry, specifically with SDTM.
What we offer:
- A collaborative and innovative work environment.
- Opportunities for professional development and career growth.
- The chance to work on impactful projects that contribute to the advancement of healthcare.
Applications are read by our talent team, usually within two working days.
If you look like a fit we will call you, and you will hear from us either way.