What are the responsibilities and job description for the Clinical Trials Analyst position at Katalyst HealthCares and Life Sciences?
Job Summary:
Katalyst HealthCares and Life Sciences is seeking a skilled Sr. Statistical Programmer to join our team. The successful candidate will be responsible for utilizing SAS to generate and validate tables, listings, and figures (TLF) based on SAP. They will also use major statistical programming languages to perform data analysis for various needs. Additionally, they will provide statistical analysis support for post-approval studies, evaluate and ensure CDISC compliance with study tabulation and analysis data files, and write specifications and statistical programs to generate analysis datasets and outputs. The ideal candidate will have strong SAS programming skills, extensive statistical programming experience, and a BS degree in Statistics, Mathematics, Computer Science, or a related field. MS in Statistics or Biostatistics is preferred.
Key Skills:
- Strong SAS programming skill in producing various types of outputs such as TLFs and datasets
- Extensive statistical programming experience in producing deliverables either on a scheduled or ad hoc basis
- BS degree in Statistics, Mathematics, Computer Science, or related field, MS in Statistics or Biostatistics is preferred
- Experience with producing outputs submitted to the FDA and other regulatory agencies
- Excellent organizational skill to prioritize multiple tasks and goals to ensure timely completion
- Attention to detail and able to adapt to a fast-paced environment
- Ability to work both independently and in a cross-functional team
- Excellent communication skills
- Sufficient knowledge in CDISC and SDTM/ADAM for FDA submission compliance
How to Apply:
Please submit your application, including your resume and cover letter, to [insert contact information]. We look forward to hearing from you.
Katalyst HealthCares and Life Sciences is seeking a skilled Sr. Statistical Programmer to join our team. The successful candidate will be responsible for utilizing SAS to generate and validate tables, listings, and figures (TLF) based on SAP. They will also use major statistical programming languages to perform data analysis for various needs. Additionally, they will provide statistical analysis support for post-approval studies, evaluate and ensure CDISC compliance with study tabulation and analysis data files, and write specifications and statistical programs to generate analysis datasets and outputs. The ideal candidate will have strong SAS programming skills, extensive statistical programming experience, and a BS degree in Statistics, Mathematics, Computer Science, or a related field. MS in Statistics or Biostatistics is preferred.
Key Skills:
- Strong SAS programming skill in producing various types of outputs such as TLFs and datasets
- Extensive statistical programming experience in producing deliverables either on a scheduled or ad hoc basis
- BS degree in Statistics, Mathematics, Computer Science, or related field, MS in Statistics or Biostatistics is preferred
- Experience with producing outputs submitted to the FDA and other regulatory agencies
- Excellent organizational skill to prioritize multiple tasks and goals to ensure timely completion
- Attention to detail and able to adapt to a fast-paced environment
- Ability to work both independently and in a cross-functional team
- Excellent communication skills
- Sufficient knowledge in CDISC and SDTM/ADAM for FDA submission compliance
How to Apply:
Please submit your application, including your resume and cover letter, to [insert contact information]. We look forward to hearing from you.
