CRA ICON plc is a world-leading healthcare intelligence and clinical research organization We re proud to foster an inclusive environment driving innovation and excellence and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Clinical Research Associate CRA to join our diverse and agile team As a Senior CRA at ICON Plc you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol regulatory requirements and industry standards You will contribute to the success of clinical trials by ensuring data integrity participant safety and compliance throughout the study lifecycle What You Will Be Doing Monitoring clinical trial sites to ensure adherence to study protocols regulatory requirements and Good Clinical Practice GCP standards Conducting site visits to assess site performance resolve issues and provide support to ensure successful trial execution Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations Your Profile Advanced degree in a relevant field such as life sciences nursing or medicine Extensive experience as a Clinical Research Associate with a strong understanding of clinical trial processes and regulatory requirements Proven ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills Expertise in monitoring practices data integrity and site management with proficiency in relevant clinical trial software and tools Excellent communication interpersonal and stakeholder management skills with the ability to influence and drive compliance within a complex environment Ability to travel at leas

📌 Cra Ii (Bengaluru)
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📍 Bengaluru