We are seeking experienced Clinical Research Associates (CRAs) with radiopharmaceutical therapeutic expertise to lead and support clinical trial monitoring for various sponsors. A minimum of 1+ year of independent CRO/sponsor monitoring is required, with flexibility across major US hubs. The role involves
Qualifications include a university or health-related certification, 1+ years of clinical monitoring experience, with radiopharmaceutical experience preferred. The role requires adaptability to fast-paced, evolving environments, strong teamwork, and proficiency with electronic data systems.
Benefits include comprehensive medical coverage, 401(k), paid time off, recognition awards, and employee resource groups. The work environment involves office settings and frequent travel, with physical requirements such as prolonged sitting, light lifting, and computer use. Applications are accepted continuously.