Principal Statistical Programmer
2 days ago
Responsibilities:
- Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
- 6 -7 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
- Statistical Programming and SAS hand-on experience
- Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.
- Good understanding of ICH and regulatory guidelines
- Working knowledge of clinical data and relevant data standards
- Strong written and oral communication skills, and project management skills
- Proven ability to operate with limited oversight
- Knowledge of at least 1 Therapeutic Area
- Proven ability to manage delivery under tight timelines.
- CDISC experience desirable
Qualifications:
Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
Required Skills:
- 6 -7 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
- Statistical Programming and SAS hand-on experience
- Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.
- Good understanding of ICH and regulatory guidelines
- Working knowledge of clinical data and relevant data standards
- Strong written and oral communication skills, and project management skills
- Proven ability to operate with limited oversight
- Knowledge of at least 1 Therapeutic Area
- Proven ability to manage delivery under tight timelines.
- CDISC experience desirable
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