Trio Clinical Resourcing, Aptiv Solutions has an exciting opportunity for a Contract Regional Site Manager (CRA) working for one of our Pharmaceutical clients out of your home office in the Omaha, NE area. The Contract Regional CRA is responsible for overseeing the conduct of clinical trials at investigative sites to ensure the quality and integrity of data and to ensure that the rights and welfare of research subjects are protected.
Key responsibilities include:
-Conduct the following monitoring visits according to applicable SOPs, Working Documents, GCP/ICH guidelines, Protocol Specific Monitoring Plans, and departmental timelines
-Manage all site activities for assigned sites
-Communicate site status and monitoring activities
You will be expected to work autonomously in a variety of situations as an integral member of the project team.
We are looking for that exceptional person who brings progress a positive attitude, a professional demeanor coupled with a focus on continuous process improvement.
To be considered for this role you must have:
-Bachelor’s degree
-5+ years regional monitoring experience with passion for monitoring
-Independent contractor with experience and interested in dedicated contract with 1 sponsor
-Live in the requested area and 1 hr from major airport
-2 + yrs and recent experience with EDC
-CNS, CV, or Respiratory preferred
-Ability to travel overnight an average of 75%
If this sounds like your ideal position, please contact me at your earliest convenience. Or if you know of a colleague exploring opportunities please forward along. carla.nelson@aptivsolutions.com, (314) 716-2064