We are seeking experienced Clinical Research Associates (CRAs) with radiopharmaceutical therapeutic expertise to lead and support full-service clinical monitoring for various sponsors.

Key Responsibilities

Include Monitoring all aspects of clinical sites, including routine visits, site close-out, study file maintenance, and vendor liaison Managing site activities per project plans and ensuring protocol adherence Verifying informed consent procedures and patient safety Ensuring data integrity by reviewing case report forms and addressing discrepancies Handling Serious Adverse Event (SAE) reporting and follow-up Training new staff and coordinating clinical projects as a Local Project Coordinator

Qualifications

And Skills Degree or certification in healthcare or related field (e.g., nursing licensure) Minimum 1+ years of clinical monitoring experience; radiopharmaceutical experience preferred Comfortable working in a fast-paced, evolving environment with strong teamwork and technological skills This role involves travel (60-70%), with work performed in an office setting and requires physical ability for site visits. Benefits include comprehensive health coverage, 401(k), PTO, and recognition programs.