Calling ALL Motivated Oncology Clinical Research Coordinators / Oncology Research Nurses!
We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.
Who are we?
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.
What's in it for you in the long term?
We promote from within We provide a career not a job.
Culture There is nothing like it. We have many former PRA employees returning every single month.
Tools and Technology Leading the industry with time saving, intuitive smart technology to help predict trends, anticipate needs and eliminate the need for multiple data entry.
Security We are growing and we are dedicated to having you grow with us.
Mentorship and Training Our structure provides support for your growth and development as well as questions that arise while on a study at all times.
Work/Life Balance It's real; we value it. Our strategic solutions and full service models offer you choices for finding a career that includes time for your personal life.
Salary/ Benefits- We are committed to providing our employees with a competitive salary and benefits package with yearly merit and performance reviews.
What will you be doing? PRA's Bridge Program pairs experienced Study Coordinators or Clinical Research Nurses 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 required or 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