Clinical Research Associate - Sponsor Dedicated

Role Overview The position involves supporting clinical studies across various therapeutic areas as a Clinical Research Associate II (CRA II) or Senior CRA. Key Responsibilities Conduct site monitoring activities including selection, initiation, routine visits, and close-out.Ensure compliance with study protocols, GCP, ICH guidelines, and regulatory standards.Collaborate with sites to develop and track patient recruitment and retention strategies.Provide protocol training and maintain communication with site staff.Identify, escalate, and resolve quality and compliance issues.Monitor study progress through tracking regulatory submissions, enrollment, and data quality.Maintain accurate documentation within TMF and ISF, prepare monitoring reports.Support study execution through cross-functional collaboration and potentially assist with start-up activities and financial management. Qualifications & Skills: Bachelor’s degree in Life Sciences, Healthcare, Nursing, or related field preferred; relevant experience may suffice.At least 2 years of independent on-site monitoring experience in the industry.Strong knowledge of clinical research processes, GCP, ICH guidelines, and therapeutic areas.Proficiency in Microsoft Office and electronic data capture tools.Excellent communication, organizational, and problem-solving skills.Ability to work independently and in team settings. Join a global leader in clinical research to contribute to innovative therapies that improve patient outcomes and advance your career.