Clinical Research Associate (Senior)

Role: Clinical Research Associate responsible for leading site monitoring activities and ensuring protocol compliance in clinical trials. Key Responsibilities Conduct site monitoring visits, including selection, initiation, routine, and close-out activities.Build and maintain strong relationships with investigative sites to enhance performance and recruitment.Ensure adherence to protocols, data integrity, and high-quality study execution.Monitor study progress by tracking regulatory approvals, enrollment, and data quality.Identify risks, resolve issues, escalate concerns, and maintain accurate documentation. Qualifications & Skills Bachelor’s degree in life sciences, healthcare, or related field.At least 1.5 years of on-site monitoring experience.Solid knowledge of GCP, ICH, and regulatory standards.Strong communication, problem-solving, and organizational abilities.Ability to manage multiple priorities in a fast-paced environment.