Job Description
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Research Associate in the United States.
This role is a field-based clinical research position focused on the independent monitoring and management of clinical trial sites, ensuring the highest standards of data integrity, regulatory compliance, and patient safety. You will be responsible for overseeing site performance across all phases of clinical studies, from start-up through close-out, within a fast-paced and highly regulated environment. The position involves frequent collaboration with investigators, site staff, and internal study teams to ensure smooth execution of protocols and adherence to GCP/ICH guidelines. You will play a key role in identifying and mitigating site risks, supporting audit readiness, and maintaining high-quality trial documentation. This is a highly autonomous role requiring strong attention to detail, excellent communication skills, and the ability to manage multiple sites and priorities. The position requires meaningful travel and offers exposure to complex therapeutic areas, including oncology and rare diseases.
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Research Associate in the United States.
This role is a field-based clinical research position focused on the independent monitoring and management of clinical trial sites, ensuring the highest standards of data integrity, regulatory compliance, and patient safety. You will be responsible for overseeing site performance across all phases of clinical studies, from start-up through close-out, within a fast-paced and highly regulated environment. The position involves frequent collaboration with investigators, site staff, and internal study teams to ensure smooth execution of protocols and adherence to GCP/ICH guidelines. You will play a key role in identifying and mitigating site risks, supporting audit readiness, and maintaining high-quality trial documentation. This is a highly autonomous role requiring strong attention to detail, excellent communication skills, and the ability to manage multiple sites and priorities. The position requires meaningful travel and offers exposure to complex therapeutic areas, including oncology and rare diseases.
