Clinical Data Associate

About the Role

This is a full-time, on-site role for a Clinical Data Associate, based in Bengaluru. The Clinical Data Associate will be responsible for managing and processing clinical trial data, ensuring accuracy and compliance with regulatory guidelines. Collaboration with cross-functional teams and maintaining data integrity are essential aspects of this role.

Key Responsibilities

• Managing and processing clinical trial data
• Coordinating and maintaining data entry
• Conducting data validation
• Preparing reports
• Supporting audit and monitoring processes

Requirements & Tech Stack

• Proficiency in managing clinical trial data
• Familiarity with Electronic Data Capture (EDC) systems
• Strong skills in data validation, data cleaning, and quality control procedures
• Understanding of regulatory requirements and Good Clinical Practice (GCP) guidelines
• Proficiency in software tools such as Excel and data management platforms
• Effective communication and teamwork skills to collaborate with cross-functional teams

Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, or related field
• Excellent organizational skills, attention to detail, and ability to multitask effectively
• Previous experience in clinical research or data management is preferred