CRA & Sr. CRA - Radiopharmaceutical Therapies - Remote

We are seeking experienced CRAs with Radiopharmaceutical therapeutic expertise to lead clinical trial monitoring for various sponsors. A minimum of 1+ year of independent CRO/sponsor monitoring is required. The role involves managing all aspects of site monitoring, including routine visits, site close-out, study file maintenance, and liaising with vendors. Responsibilities include ensuring protocol adherence, patient safety, informed consent, data integrity, SAE reporting, and training staff. The position requires a university degree or allied health certification, 1+ years of clinical monitoring experience, and preferred radiopharmaceutical knowledge. Candidates should be adaptable to a fast-paced environment with changing priorities, possess strong teamwork and communication skills, and be comfortable working with electronic data collection. Open to various hub locations across the US, with significant travel involved. Benefits include comprehensive health coverage, 401(K), PTO, recognition awards, and ERGs. The work environment involves office-based tasks with frequent travel, requiring physical ability for extended sitting, light lifting, and computer use. Applications are accepted continuously.

Work arrangement
Yes