Work with both experienced and research naïve investigators.
Either through online or in-person you can be trained in Good clinical practices and FDA guidelines that govern clinical trials.
Learn what sponsors look for in a Principal investigator.
Help you identify staffing necessary for this vital role
Train your M.A. or Nurse to become a Certified Clinical Research Coordinator
Obtain trials appropriate for your site’s population and specialties
Leverage years of experience and Key Contacts in the field to bring you the latest trials.
Prepare IRB Submissions
Write Investigator initiated Proposals
Budget & Contract Management
Negotiate highest budgets for your trials.
Ensure your site is indemnified and all contracts are in line with malpractice standards
Help you choose which CTMS platform is right for you
Launch CTMS and integrate it with your EMR
G2 can run a small protocol from start to finish. Services include:
Obtaining IRB approval
Patient recruitment & overall project management