Our Clinical Research Professionals are highly experienced. The majority
of CRMi monitors have more than a decade of successful field experience in
a wide range of therapeutic areas.
CRMi Project Managers undergo rigorous training, and have all come up through
the CRA ranks. They know exactly what it takes to make a program successful
in the real world.
CRMi Medical Officers have extensive expertise in evaluating, managing and
reporting safety information for IND programs, NDA/BLAs, and Postmarketing
Surveillance.
Our team of well-trained and detail-oriented GCP Auditors provide site auditing
services for study closeouts, NDA/BLA preparation, as well as pre-emptive
audits for cause.
CRMi also provides ongoing Regulatory Affairs, CMC, and Preclinical support
to clients on a project or program-specific basis through our network of
affiliated Regulatory Affairs and Development Professionals.
Clinical
Operations / Project Management
