Principal Statistical Programmer Opportunity at Clario

Are you seeking a purposeful and rewarding SAS programming career? Join our growing statistical programming team in India! At Clario, we have big ambitions and a clear vision for the future. Now is the perfect time to become part of our journey.

What We Offer

• Competitive Compensation
• Attractive Benefits (security, flexibility, support, and well-being)
• Engaging Employee Programs

Role Responsibilities

As a Statistical Programmer at Clario, you will:

• Create, test, and maintain SAS codes for generating CDISC compliant datasets for cardiac safety statistical analysis.
• Develop and maintain procedures for ADaM dataset creation and generate electronic submission packages for cardiac safety submissions.
• Support statistical programming activities for assigned cardiac safety studies by creating dataset specifications.
• Participate in SAS programming process improvement and mentor new employees.
• Perform all necessary functions to meet corporate commitments and deliverables, particularly in coding for statistical datasets using SAS.
• Review and create electronic submission deliverables for sponsor submissions.
• Create and maintain SAS codes for analysis datasets, including programming specific flags and specifications per the Statistical Analysis Plan.
• Develop submission-ready datasets for cardiac safety trials (SDTM EG and ADaM ADEG), collaborating with the client, internal statistics, and data management teams to ensure CDISC standards compliance.
• Keep current with CDISC standards and recommend process improvements and standard specification changes as needed.
• Create define.xml and dataset reviewers guide for FDA submissions, referencing the datasets created for statistical analysis.
• Assist statisticians in preparing Tables, Listings, and Figures for cardiac safety studies.
• Assist in orienting and training new statistics team members, systems analysts, and data management personnel as determined by management.
• Collaborate with the whole department to recommend, develop, and implement SOPs for improved procedures within the statistics group.

Candidate Qualifications

We are looking for candidates with the following qualifications:

• BS in Computer Sciences, Engineering, Statistics, or Mathematics.
• Experience with CDISC SDTM and ADaM standards.
• At least 10 years of experience with SAS products and procedures, preferably in a pharmaceutical or life sciences setting.
• Understanding of pharmaceutical drug development gained through a minimum of two years of experience in the pharmaceutical or healthcare industry.
• Strong organizational, analytical, and communication skills.
• Detail-oriented with proficiency in Windows and Microsoft Office products.
• Experience generating TFLs is a plus.
• Ability to work effectively in teams and within a matrix organization.
• Excellent interpersonal skills to contribute to team spirit.
• Ability to anticipate and respond to customer needs and inquiries.
• Excellent time management, organization, and prioritizing skills.

Join Clario and be part of a dynamic team driving forward with a clear vision for the future. We look forward to receiving your application.