Gen1’s dedicated Life Science team focuses their efforts on trial acquisition, maintaining a steady pipeline of trials offered. Our trial selection process is thorough and thoughtful, with your interests, specialties, and patients driving the decision. We primarily work with Phase 2, 3, and 4 trials in 10 different therapeutic areas. Training, budgeting, compliance: we do it all to get the trial up and running. During the trial, a Clinical Research Coordinator (CRC) is always present, ensuring the research is being conducted appropriately. Our sites are compensated on a quarterly basis.
We have found that it is ideal to have a dedicated research room at each site. Gen1 requires a non-compete to be in place. If the protocol is followed appropriately and an Adverse Event or Severe Adverse Event occurs, then ultimately the sponsor producing the study drug is liable. NP or PA can be Sub-Investigators, but not Principal Investigators. Upon completion of a clinical trial, Gen1 Research will handle all data reporting and other steps necessary to officially close out the trial.
Research in your clinic
We bring all the necessary tools and resources directly to your own practice.
Conducting research is not only free of cost, but creates new revenue streams for your practice.
Focus on your patient
We provide end-to-end trial management, so you can concentrate on caring for your patients.