What We Do Protocol Management by experimental clinical research coordinators Click Here Trial-related documents archival and maintenance Click Here Patient informed consent form (ICF) Click Here Timely submission for Institutional Review Board (IRB) approval Click Here Contract negotiations with the clinical drug trials accountability and integrity Click Here Compliance patient counselling Click Here Advising & Alerting of potential protocol violations Click Here Site initiation and trial close-out operational Click Here Reporting serious adverse events to the sponsor or CRO and the IRB/IEC Click Here Patient recruitment Click Here Patient follow-up Click Here
