Senior Statistical Programmer Consultant
C
ClinChoiceClinical Research CRO
Location: United KingdomContractSenior
Salary not disclosed
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Job Details
- Experience
- 5 yrs. of clinical programming experience with a Bachelor's degree, or 6 yrs. with a Master's degree.
- Required Skills
- GCP
Requirements
- Bachelor’s degree in CS, statistics, or related discipline with 5 years of clinical programming (CDISC) experience
- Master’s degree in CS, statistics, or related discipline with 6 years of clinical programming (CDISC) experience
- Strong SAS programming experience within the pharmaceutical/CRO industry
- Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
- Experience in Respiratory/Immunology therapeutic areas
- Experience in generating and validating SDTM, ADaM, and TLFs
- Good understanding of CDISC standards and clinical trial processes
- Working knowledge of ICH and Good Clinical Practices (GCP)
- Strong communication and stakeholder management skills
- Ability to work independently and manage multiple priorities
Responsibilities
- Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
- Create datasets, tables, listings, and figures according to study requirements
- Collaborate with Biostatistics, Data Management, and Clinical teams
- Ensure programming deliverables meet quality standards and project timelines
- Participate in study planning, review specifications, and support submission activities
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