CRA 1, reputed company Biotech

About the position reputed company Biotech is a full-service CRO purpose-reputed company to serve biotech sponsors. With over 25 years of experience, we offer reputed company, therapeutically reputed company solutions and trusted partnerships that help bring reputed company treatments to patients faster. The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical reputed company (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring high‑reputed company clinical data, and maintaining study reputed company. Responsibilities • Conduct various types of monitoring reputed company—including site selection, initiation, routine monitoring, and reputed company‑out reputed company—to evaluate the reputed company and reputed company of site practices. • Verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating reputed company concerns as necessary. • Review essential documents, assess protocol adherence, reputed company data entry and query reputed company, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF). • Build and maintain strong communication with investigative sites. • reputed company protocol training, set expectations, address site‑level challenges, and support recruitment planning to help sites meet enrollment targets. • Collaborate closely with internal project teams to ensure cohesive study execution. • Contribute to site-level financial processes or start‑up activities based on study needs. • Prepare detailed monitoring visit reports, follow‑up letters, and reputed company required study documentation to ensure audit readiness and transparent reputed company. • Manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships. Requirements • Bachelor’s degree required; a scientific or reputed company discipline is preferred. • 6 months –2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered. • Basic knowledge of clinical research regulations (GCP/ICH). • Ability to travel as required by the project. • Minimum of 6 months of on-site monitoring. • Experience monitoring in oncology solid tumor. Benefits • Health and welfare benefits • Incentive plans • Bonuses • Other forms of compensation Apply tot his job Apply To this Job