Who are you?
You are a Clinical Research Coordinator, a site-level clinical trial wizard, eager to apply your expertise in a Clinical Research Associate role. You are a forward thinker.
You are an innovator that refuses to settle. You want to push the boundaries and change not just what it means to be a Clinical Research Associate, you want to change the future. You want to learn from the best, grow your knowledge and your skill set, and you want to build your career here.
You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you're more than an employee number. A place you love working.
Still here? Good. Because if this is you, we'd really like to meet you.
What will you be doing? PRA's Bridge Program pairs experienced Study Coordinators with veteran CRAs to learn the art and science of monitoring.
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.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? * Undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution; a licensed healthcare professional (ie, registered nurse)* 2+ years of Study Coordinator or Clinical Research Nurse experience with subject matter expertise in Oncology or other equivalent Oncology experience
PRA Health Sciences