The CRPM will train and supervise research staff, manage a portfolio of clinical trials, and develop and/or contribute to standard operating procedures and processes. This individual will attend and engage in leadership meetings, oversee research operations in the department, and provide expert consulting at an institutional level. Occasionally will meet with patients in the clinic.
3 years of clinical research experience (doesn't have to be PM experience) and a Master's Degree or 5 years and a Bachelor's Degree
Experience working on interventional clinical trials
Experience overseeing protocol development process and management of clinical trials
Experience working directly with patients
Previous experience managing people, conducting 1 on 1s performance reviews, and providing direction
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.