Clinical Data Management Specialist

IQVIA; Bengaluru; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

IQVIA is seeking a Mid Level SAS Programmer in Bengaluru to develop, validate, and maintain SAS programs for clinical study deliverables. You will generate and review Data Validation Listings to ensure data accuracy, completeness, and consistency.

Join a cross-functional team collaborating with Data Management, Biostatistics, and Clinical Operations to support study milestones while adhering to regulatory standards. Strong SAS Macros/SQL skills and attention to quality are essential.

Qualifications

• Strong proficiency in SAS programming.
• Experience developing and reviewing Data Validation Listings (DVLs).
• Good understanding of clinical trial data and programming standards.
• SAS Macros and SQL proficiency; strong analytical and communication skills.

Responsibilities

• Develop, validate, and maintain SAS programs for clinical study deliverables.
• Generate and review Data Validation Listings (DVLs) to ensure data accuracy and consistency.
• Support creation and maintenance of clinical data outputs, reports, and listings.
• Collaborate with Data Management, Biostatistics, and Clinical Operations; ensure quality and standards.

Skills

SAS programming

Data Validation Listings

SAS Macros

SQL

Analytical skills

Communication skills

Tools

SAS

SQL

Job description

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Experience Level Mid Level