Overview:
The responsibility of this position is to provide clinical expertise when appropriate to both Department of Site and Study Management (DSSM) staff and DSSM member institutions. To assist with the facilitation of new Phase I, II, and III industry funded clinical trials from concept through development and launch and continue throughout the life of the trial. She/he will act as a clinical resource to answer queries regarding all aspects of the clinical trial. The individual will also conduct medical review, determine protocol eligibility, and review adverse events and reporting when applicable. In addition, the candidate will participate in the development of educational programs for DSSM member institutions.
This position reports directly to the Senior Director of the Department of Site and Study Management.
Ideal Candidate will have:
• 3-5 years Oncology research experience
• The ability to work autonomously with minimal supervision on multiple projects
• Knowledge of regulatory standards, FDA and GCP for industry trials
• Bachelor degree and RN licensure in PA
• Proficiency in Microsoft Office applications
This position is full-time, Monday-Friday daylight hours. Competitive salary plus an outstanding benefits package. Employee focused company that offers work-life balance and opportunity for long-term professional growth.
