We are seeking experienced Clinical Research Associates (CRAs) with radiopharmaceutical therapeutic expertise to lead and support our Full Service Outsourcing team across various sponsor projects. A minimum of 1+ year of independent CRO/sponsor monitoring is required, with open hub locations across the US and 60-70% travel expected.
Key responsibilities include:
- Monitoring all aspects of clinical studies, including site initiation, routine visits, close-out, and vendor liaison
- Managing study site activities and ensuring adherence to protocols and regulatory standards
- Verifying informed consent procedures, maintaining study files, and ensuring data integrity
- Handling SAE reporting, data review, and query resolution
- Training new staff, coordinating clinical projects, and acting as a local client contact
Qualifications:
- Degree or certification in a related health field (e.g., nursing licensure)
- 1+ years of clinical monitoring experience; radiopharmaceutical experience preferred
- Comfortable working in a fast-paced, dynamic environment with changing priorities
- Strong teamwork, communication, and technology skills
Benefits include: comprehensive health insurance, 401(K), PTO, recognition awards, and employee resource groups. The role involves office work and frequent travel, with physical requirements such as sitting, lifting light objects, and computer use. Applications are accepted continuously.