Job Type: Permanent
Specialism: Data Management Detail Oriented Operations Problem – Solving Statistical Knowledge
Industry: CRO & Clinical Operations
Salary: $100000 - $120000
Location: USA
ClinicalPro is seeking a Senior SAS Programmer for a leading CRO located in the USA.
This individual will be responsible for offering statistical programming support for a number of clinical studies and related tasks.
Must be eligible to work in the USA.
Responsibilities
- Serves as the project’s main programmer and offers assistance with programming and statistics for one or more Phase I–III clinical trials.
- Create analytical datasets, tables, lists, and figures using SAS programmes.
- Create, verify, and manage a mapped database using SAS.
- Programme revision verifies external data.
- Make annotated CRF to STDM datasets and review them.
- Assemble and keep up with technical programming specification documentation.
- Organise and take the lead in client and project review meetings.
- Discuss study protocol or statistical analysis concerns with clients.
- Validate statistical outputs.
- Oversee the statistical techniques applied.
- Maintain industry standards and legal obligations.
- Encourage the creation and use of suitable statistical techniques in clinical research.
- Work with Data Management to coordinate communications and concerns related to database requirements and data transfers.
Skills and Requirements
- MS or PhD in statistics, biostatistics, or a closely related discipline.
- 5+ years’ experience in the CRO, biotech, pharmaceutical, or life sciences industries in a related job.
- Understanding of regulatory guidelines (FDA/EMA, ICH/GCP) and experience with clinical trial design and analytic tasks.
- Having knowledge of the NDA/BLA submission process.
- Knowledge of statistical software, including the Statistical Analysis System (SAS), CDISC, and SDTM.
- Knowledge of the Ultra Compare programme.
- Keep abreast with departmental policies, legal requirements, industry standards, and Standard Operating Procedures (SOPs).
- Excellent time management, workload prioritisation, and deadline-meeting abilities.
- Excellent interpersonal and communication abilities to successfully communicate with others.
Apply
If you’re interested in this position, apply now to send us an updated copy of your CV, or give us a call right away.
To explore more opportunities, visit Opportunities at ClinicalPro