Who are you?
You are dedicated to clinical research and have a passion for oncology clinical trials. You thrive in a busy environment, multi-tasking between patient engagement, data entry and regulatory responsibilities required with oncology clinical trials. You want to help improve lives and you are dedicated to detailed, quality clinical trial work. Often known as the go to person, you understand the intricacies of oncology clinical trials and are hands on in all facets of an oncology clinical trial. You want to learn from the best, grow your knowledge and your skill set, and you want to build your career here. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.
What is Bridge?
PRA hires experienced oncology clinical trial coordinator/study coordinators or clinical research nurses and marries that oncology expertise with our exceptional CRA training program to become an oncology CRA monitor. Bridge hires will attend an intensive two week, instructor-led training course in our Corporate office in Raleigh, NC. Our highly-trained CRA mentors provide on-the-job training, working closely and meeting weekly with the new CRAs.
What will you be Doing?
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
What do you need to have?
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.