IQVIA
Website:
iqvia.com
Job details:
Job Title: SAS Programmer
Experience: 3+ years.
Location: Home - based
Primary Skill: Clinical SAS, Edit checks, reconciliation, patient profile generation etc.
Job Description Summary:
Key Responsibilities: -
- Develop, validate, and maintain SAS programs for clinical study deliverables.
- Generate and review Data Validation Listings (DVLs) to ensure data accuracy, completeness, and consistency.
- Support the creation and maintenance of clinical data outputs, reports, and listings.
- Apply programming best practices, including code optimization, documentation, and quality control.
- Collaborate with cross-functional teams including Data Management, Biostatistics, and Clinical Operations.
- Utilize SAS macros and SQL programming to automate and streamline processes.
- Participate in data review activities and contribute to issue resolution.
- Support study milestones and timelines while ensuring adherence to regulatory and company standards.
Required Qualifications: -
- Strong proficiency in SAS programming.
- Hands-on experience in developing and reviewing Data Validation Listings.
- Good understanding of clinical trial data and programming standards.
- Working knowledge of SAS Macros and SQL.
- Strong analytical, problem-solving, and communication skills.
- Demonstrated understanding of programming best practices and quality standards.
Preferred Qualifications: -
- Experience with Protocol Deviation Listings and Patient Profile generation.
- Knowledge of the Clinical Data Management (CDM) full lifecycle.
- Exposure to Power BI for data visualization and reporting.
- Experience working in regulated clinical research environments.
Desired Skills: -
- Clinical Data Programming
- SAS Base, SAS Macros, SQL
- Data Validation & Quality Control
- Protocol Deviations
- Patient Profiles
- Clinical Data Management (CDM)
- Power BI (Preferred)
- Team Collaboration & Stakeholder Communication
Click on Apply to know more.
