Job Description

We are seeking a skilled and detail-oriented Clinical SAS Programmer to join our clinical research team. The Clinical SAS Programmer will play a key role in analyzing and reporting clinical trial data using SAS software. The ideal candidate will have a strong background in SAS programming, clinical data management, and a thorough understanding of regulatory requirements in the pharmaceutical or healthcare industry. Responsibilities:

• Collaborate with cross-functional teams, including biostatisticians, data managers, and clinical research associates, to develop programming specifications and data analysis plans.
• Design and develop SAS programs to generate tables, listings, and graphs (TLGs) for clinical study reports, regulatory submissions, and other study-related documents.
• Perform data validation and quality control checks to ensure accuracy and integrity of clinical trial data.
• Create and maintain SAS datasets, including data transformation, cleaning, and integration from multiple sources.
• Develop and validate SAS macros and utilities to automate repetitive tasks and improve programming efficiency.
• Ensure compliance with regulatory guidelines, industry standards, and company SOPs in programming and data handling.
• Collaborate with statisticians to provide input on statistical analysis plans and assist with statistical programming tasks as needed.
• Conduct ad-hoc data analyses and generate reports in response to internal and external requests.
• Participate in data review meetings and provide support for data-related queries from internal and external stakeholders.
• Stay updated on emerging trends, new methodologies, and advancements in SAS programming techniques.
• Document programming processes, datasets, and programming specifications in accordance with company standards.
• Contribute to process improvement initiatives and share best practices within the programming team.

Qualifications and Skills:

• Bachelor\'s or Master\'s degree in a relevant scientific discipline (e.g., statistics, biostatistics, computer science).
• Minimum of 3 years of experience as a Clinical SAS Programmer in the pharmaceutical, biotech, or clinical research industry.
• Proficiency in SAS programming, including SAS/Base, SAS/STAT, SAS/Graph, and SAS/Macro.
• Strong understanding of clinical trial data structures, CDISC standards (SDTM and ADaM), and regulatory guidelines (e.g., ICH-GCP).
• Experience in generating TLGs, tables, and figures for clinical study reports and regulatory submissions.
• Solid knowledge of data management principles and processes.
• Familiarity with data visualization tools and techniques.
• Excellent problem-solving and analytical skills.
• Detail-oriented with the ability to work on multiple projects and meet deadlines.
• Good communication and interpersonal skills to collaborate effectively with cross-functional teams.
• Knowledge of programming languages such as Python or R is a plus.
• Certification in SAS programming or clinical data management is desirable.

Salary and Benefits:

• Competitive salary based on qualifications and experience.
• Professional development opportunities to enhance SAS programming skills and knowledge.

Job Types: Full-time, Fresher Salary: From 925,000.00 per month Benefits:

• Cell phone reimbursement

Schedule:

• Day shift
• Morning shift

Supplemental pay types:

• Commission pay
• Performance bonus

Ability to commute/relocate:

• Bangalore, Karnataka: Reliably commute or planning to relocate before starting work (Required)

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