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.
Who we are?
We Are PRA. We are 16,000+ employees strong, operating in more than 90 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most.
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 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?
Must be located near one of the following major international airports: Boston, New York City, New Jersey, Philadelphia, Baltimore, DC, Ft. Lauderdale, Miami, Houston, Nashville, Detroit, Chicago, St. Louis, Birmingham, Atlanta, Pittsburgh, Columbus or Denver.
Highly Preferred undergraduate degree or its international equivalent in clinical, science or health related field from an accredited institution required OR a licensed healthcare professional (ie, Registered Nurse)
3+years of Study Coordinator or Clinical Research Nurse with hands on ONCOLOGY CLINICAL TRIAL experience required
Must be able to travel up to 80% weekly
60 mins from major international airport
To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities
About PRA HealthSciences
Who are we?
We Are PRA Health Sciences. We provide innovative drug development solutions across all phases and therapeutic areas. But innovation just for the sake of innovation isn’t why we do it. Side by side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every day. It’s who we are. Innovating to help people is at the heart of our process, but it’s even more than that. It’s our privilege.
We are 15,000+ employees strong, operating in more than 85 countries. We are committed to saving lives, and we are constantly striving to be the best at what we do.