Clinical Research Associate

Auriga Research Private Limited (ARL), established in 2007, is a renowned Contract Research Organization (CRO) providing end-to-end services for the pharmaceutical, biological, herbal, cosmetic, nutraceutical, and medical device industries. With expertise in Clinical Trials, Pharmacovigilance, Clinical Data Management, and Cosmetic Studies, the company supports the entire product lifecycle from development to regulatory approvals. Leveraging advanced systems like Clinical Trial Management System (CTMS) and electronic Trial Master File (eTMF), ARL ensures compliance with Good Clinical Practice (GCP) and delivers high-quality data and results. Backed by strong Quality Management Systems (QMS), the company maintains rigorous standards and aims to simplify complex regulatory processes, ensuring timely and efficient market access for innovative products.

This is a full-time, on-site position for a Clinical Research Associate based in Manesar. The role involves overseeing clinical trials, ensuring compliance with study protocols and regulatory requirements, managing Site Initiation Visits (SIV), monitoring trial progress, and ensuring quality data collection and reporting. The position also requires collaboration with clinical sites, managing investigator relationships, and performing site closeout activities.

• Knowledge of Clinical Trials, Clinical Data Management, and Good Clinical Practice (GCP)
• Familiarity with regulatory processes and guidelines, including national and international standards
• Experience in Site Management, Site Initiation, and Site Monitoring
• Proficiency in data documentation, statistical analysis, and use of tools such as CTMS and eTMF
• Strong organizational, communication, and problem-solving skills
• Ability to work on-site in Manesar and travel as needed for trial-related activities
• Educational background in life sciences, pharmacy, or related fields; a master's degree is a plus
• Experience in pharmacovigilance, bioequivalence studies, or cosmetic safety trials is advantageous