SAS Programmer

IQVIA India; Bengaluru; Hybrid; INR 800,000 - 1,100,000; Full time

Job summary

IQVIA India seeks a Clinical Programmer to support Biomedical data management activities and collaborate with cross-functional teams in a hybrid model across India.

The role focuses on ensuring data quality, regulatory-standard reporting, and timely delivery of study outputs, leveraging Clinical SAS and SAS Macros in a collaborative environment.

Qualifications

• Excellent verbal and written communication skills.
• Understanding of pharmaceutical clinical development and regulatory submissions.
• Knowledge of statistics concepts and clinical data management basics.

Responsibilities

• Collaborate within Biometrics to support Clinical Data Management activities.
• Coordinate with Statistical Programmer, CDM, Biostatistician and vendors to meet project timelines.
• Ensure completeness and correctness of clinical data and data structures.

Skills

Communication skills

Analytical thinking

Cross-functional collaboration

Education

Bachelor's degree in Mathematics or Computer Science

Tools

SAS

SAS Macros

Clinical SAS

Job description

Overview

Work location: Any IQVIA office Location In India

Work Mode: Hybrid

Must Have Skills: Clinical SAS/DM SAS/SAS Macros

Note: this position is not for Statistical programming

Job Description

• Works collaboratively within Biometrics assisting in providing support to Clinical Data Management activities.
• Works collaboratively with Statistical Programmer, Clinical Data Manager, Biostatistician, Global Drug Safety, Regulatory and Project Management staff and vendors to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting.
• Ensures completeness, correctness and consistency of clinical data and data structure.
• Provides timely support to the study team on all programming matters according to the project plan and programming specification using internal standards and guidelines.
• Provides input on clinical data validation specifications and data transfer specifications.
• Contributes to the reporting of routine clinical data through regulatory approval, product launch and annual reports.
• Contributes to the monitoring of data quality during study conduct, providing information on issues along with proposed solutions.
• Acts as Study Clinical Programmer
• Reviews and accepts work by supporting Clinical Programmer
• Attend Study Meeting Team to provide inputs as needed.
• Provides guidance to timeline for deliverables.
• Performs extract, map, transform, and load of clinical data.
• Generates edit checks, listings and reports.
• Performs study tasks.

Requires a minimum of Bachelor’s degree in Mathematics (or equivalent) / Computer Science.

Qualifications

• Excellent verbal and written communication skills and interpersonal skills are required.
• Working understanding of pharmaceutical clinical development and ability to provide programming support for NDA and other regulatory submissions.
• Working understanding of statistical concepts and techniques is expected.
• Working understanding of development, validation, execution, maintenance, documentation, and archival of clinical data targeted for regulatory submission is required
• Working knowledge of FDA regulations (particularly 21 CFR Part 11), web-based Electronic Data Capture (EDC) and clinical data management systems is also required.
• Working knowledge of clinical study is required and biomarker data is preferred.