Clinical Research Associate

Responsibilities Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials Ensuring protocol compliance, data integrity, and patient safety throughout the trial process Collaborating with investigators and site staff to facilitate smooth study conduct Performing data review and resolution of queries to maintain high-quality clinical data Contributing to the preparation and review of study documentation, including protocols and clinical study reports Requirements Bachelor's degree in a scientific or healthcare-related field Minimum of 2 years of experience as a Clinical Research Associate In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines Strong organizational and communication skills, with attention to detail Ability to work independently and collaboratively in a fast‑paced environment Willingness to travel as required (approximately 60%) Core Competencies Demonstrates expertise in clinical trial processes, including site qualification, monitoring, and compliance with ICH‑GCP guidelines. Strong ability to ensure data integrity and patient safety while collaborating effectively with investigators and site staff. #J-18808-Ljbffr Jobtailor