Are you an Experienced Research Nurse, Clinical Trial Coordinator, or Clinical Study Coordinator? Join Labcorp Drug Development Monitoring Excellence Academy (MEA) and train to be a CRA. If you bring the Oncology therapeutic expertise, we will train you to be a top-notch CRA.
Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, the conduct of pre-study and initiation visits, with or without guidance; liaise with vendors; and other duties, as assigned
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
Perform CRF review, query generation and resolution against established data review guidelines, with or without direct supervision, on Labcorp Drug Development or client data management systems, as assigned by management
What Our MEA CRAs Have To Say
"My MEA training remains an amazing experience and I don't feel as though I will ever stop learning. And that is a GREAT feeling!"
"MEA is fast-paced, focused, and best of all a family. At the heart of the program are its support and adaptability."
"Everyone in MEA takes pride in their work and makes the effort to be available every step of the way. I never felt alone through the Experience and I can honestly say I have never felt more prepared and supported in any job throughout my career."
Come join the Labcorp Drug Development team, where you can help impact the lives of millions!
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements
Basic understanding of the clinical trial process
Valid driver's license
A minimum of 2 years of experience in a related field (i.e. site management, in-house CRA, study coordinator, research nurse, etc.)