We are seeking experienced Oncology Clinical Research Associates (CRAs) to lead and support clinical trial monitoring for various sponsors in a fast-paced, technology-driven environment.
Key responsibilities include:
- Managing all aspects of site monitoring, including routine visits, close-outs, study file maintenance, and vendor liaising.
- Ensuring proper site management, staff training, and adherence to protocol and regulatory requirements.
- Verifying informed consent procedures, data integrity, and safety reporting, including Serious Adverse Events (SAEs).
- Performing source document review, data query resolution, and assisting with feasibility studies and registry management.
- Supporting training of new team members and coordinating clinical projects as a Local Project Coordinator.
Qualifications and skills include:
- University degree or related health profession certification (e.g., nursing license).
- 1+ years of clinical monitoring experience, preferably in oncology and CAR-T therapies.
- Strong clinical judgment, adaptability to changing priorities, teamwork, and excellent communication skills.
- Comfort with electronic data collection and working in a high-speed environment.
This role involves significant travel (60-70%) and requires physical capability for site visits and data management tasks. Benefits include comprehensive health coverage, 401(k), PTO, and recognition awards.