CRA I/CRA II

Job description

Join Fortrea as a Clinical Research Associate and play a key role in advancing impactful clinical research. In this position, you will support the execution of clinical studies that contribute to improving global patient health and driving innovation in life sciences. Key Responsibilities: ​ - You will conduct all aspects of study site monitoring, including routine visits, initiation, and close‑out activities. - You will oversee site management activities in alignment with project plans and SOPs. - You will ensure study staff are properly trained and equipped to conduct the protocol safely and accurately. - You will safeguard patient safety by verifying informed consent and adherence to protocol and regulatory requirements. - You will review source documentation to ensure data integrity and identify missing or inconsistent data. - You will manage monitoring tasks efficiently and in line with Fortrea policies, including economical travel planning. - You will maintain audit‑ready site documentation. - You will prepare clear and timely monitoring visit reports. - You will collaborate with internal teams to assess project needs, timelines, and resources. - You will act as a point of co...