Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Trial Associate based in the United States.
This role plays a key supporting function within clinical operations, contributing to the successful execution of clinical studies across all phases, from start-up through close-out. You will be part of a highly collaborative study team focused on developing innovative oncology therapies with the potential to transform patient outcomes. The position provides essential operational, tracking, and administrative support to ensure studies run smoothly, remain compliant, and meet quality and regulatory standards. You will work closely with cross-functional stakeholders, including clinical leads, vendors, and site teams, helping maintain study documentation, manage essential systems, and support inspection readiness. The environment is fast-paced, detail-oriented, and mission-driven, with a strong emphasis on accuracy, organization, and communication. This is an opportunity to contribute directly to cutting-edge radiopharmaceutical clinical research while building strong foundations in clinical trial operations.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Trial Associate based in the United States.
This role plays a key supporting function within clinical operations, contributing to the successful execution of clinical studies across all phases, from start-up through close-out. You will be part of a highly collaborative study team focused on developing innovative oncology therapies with the potential to transform patient outcomes. The position provides essential operational, tracking, and administrative support to ensure studies run smoothly, remain compliant, and meet quality and regulatory standards. You will work closely with cross-functional stakeholders, including clinical leads, vendors, and site teams, helping maintain study documentation, manage essential systems, and support inspection readiness. The environment is fast-paced, detail-oriented, and mission-driven, with a strong emphasis on accuracy, organization, and communication. This is an opportunity to contribute directly to cutting-edge radiopharmaceutical clinical research while building strong foundations in clinical trial operations.