Senior SAS Programmer
Senior SAS Programmer
Posted on :
13-07-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
Responsibilities:
- The Senior SAS Programmer will be responsible for statistical programming for the clients clinical studies.
- In this role you will develop and validate SAS programs for data presentation analyses and provide programming support to project team members.
- Our Ideal candidate will have a strong work ethic capable of thriving in a high growth fast paced and intellectual environment.
- Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I-III clinical studies.
- Design and perform quality checks on analysis datasets tables listings figures (TFL) and written reports to support clinical trial results using SAS.
- Create and review annotated CRF to STDM datasets.
- Produce and maintain technical programming specification documents.
- Lead and actively participate in client and project review meetings.
- Communicate with clients regarding study protocol or statistical analysis issues.
- Validate statistical deliverables and ensure that appropriate statistical methods are utilized.
- Ensure adherence to industry standards and regulatory requirements.
- Facilitate the development and application of adequate statistical methods in clinical research.
- PhD or MS degree in Statistics Biostatistics or related field.
- 5 years of relevant work experience in CRO biotech pharmaceutical or life sciences industry.
- Familiarity with clinical trial design and analysis activities and knowledge of regulatory guidelines (FDA/EMA ICH/GCP).
- Experience with NDA/BLA submission activities.
- Experience in statistical programs such as Statistical Analysis System (SAS) CDISC and SDTM.
- Maintain awareness of industry standards regulatory requirements departmental guidelines and Standard Operating Procedures (SOPs).
- Excellent organizational skills time management ability to prioritize workload and meet deadlines.
- Excellent communication and interpersonal skills to effectively interact with others.
Employment Type
Full Time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
