Drug Safety Associate

ClinEra Research is a leading clinical research organization dedicated to bridging the gap between scientific innovation and clinical application. Known for its commitment to Clinical Excellence, ClinEra Research employs advanced methodologies, state-of-the-art technologies, and robust data management to ensure precise, high-quality outcomes. With a strong focus on regulatory compliance and operational expertise, the organization provides seamless support to its partners in navigating the complexities of modern medicine. Specialized in clinical trials, data management, regulatory affairs, and research innovation, ClinEra Research is shaping the future of healthcare solutions.

The Drug Safety Associate will oversee and manage various aspects of drug safety and pharmacovigilance. This full-time role involves responsibilities such as compiling and analyzing data, preparing safety reports, conducting quality checks, and ensuring compliance with regulatory standards. The Drug Safety Associate will also engage in medical coding and contribute to developing accurate and comprehensive narratives. This is an on-site position based in Bengaluru.

• Expertise in drafting high-quality narratives and ensuring accurate documentation.
• Proficiency in performing Quality Control checks to maintain precision and compliance.
• Knowledge of Regulatory Affairs processes and requirements for drug safety and pharmacovigilance.
• Background in Pharmacy or medical sciences is essential, with relevant academic or professional qualifications.
• Familiarity with Medical Coding and its application in drug safety operations.
• Strong analytical and problem-solving skills.
• Detail-oriented and capable of working in a structured, regulatory-compliant environment.
• Excellent communication skills, both written and verbal.