Role: Life Science : SAS Programmer : SDTM/ ADAM /TLF : Max 25 LPA : Apply
Industry Type: BPM / BPO
Department: Healthcare & Life Sciences
Employment Type: Full Time, Permanent
Role Category: Healthcare & Life Sciences - Other
UG: Any Graduate
Hi,
We are hiring for one of India's leading IT & consulting organizations for the position of SAS Programmer Role.
Summary:
A SAS Programmer is a data professional who uses the Statistical Analysis System (SAS) software to manipulate, manage, analyze, and report on large datasets. They create, test, and maintain code for data analysis, particularly within the pharmaceutical, clinical trial, and financial industries. Common synonyms include Statistical Programmer, Clinical SAS Programmer, or Data Analyst.
- To Apply for above SAS Programmer, WhatsApp 'Hi' @ 9519459922
- When Asked For The job Code, Type: Job Code # 9
Key Skills:
- At least 10 years of experience as SAS Programmer and minimum 1 year experience with SDTM/ ADAM/ TLF
- In depth experience in using SAS for data derivation/transformation.
- SAS Certified mandate
- Any Graduate
Key Responsibilities
- Work collaboratively with team members on a daily base
- Participate in team meetings
- Independently work directly with Data Management Lead to gather requirements, including F2F/video conferences
- Translate requirements to design, program and execute SAS codes to analyze, graph, derive and report analytical data for regulatory submissions
- Working knowledge of bio-pharmaceutical industry, specifically in the new drug development analytical / laboratory space
- Develop SAS edit checks for data cleaning/derivation
- Based on scientific and compliance principles in data derivation/transformation
- Extracting and merging data to generate standard CMC eCTD data tables, adhering to group standards
- Performing ad-hoc data reporting e.g. statistical analyses, metrics, plots
- Perform standard statistical analyses for shelf-life estimation
- Provide draft output within 24 hours for internal review
- Provide documentation of programs and projects adhering to regulatory and company standards
- Manage multiple projects with overlapping timelines and deliverables simultaneously
- Escalate issues to Project Lead directly and timely (within 1 day)
- Complete all required training timely
- Adhere to SOPs and GMP regulations