Physicians(MDs/DOs)
Provide your patients access to innovative treatment opportunities and grow your practice and reputation by taking part in ongoing leading-edge research. Chase your scientific interests, be on the leading edge of your therapeutic area of expertise, and be recognized as a leader within the medical community and potentially be part of the next discovery all while earning additional compensation for seeing patients you already treat in your practice.
ACRI is very enthusiastic to connect each respective physician and clinical research site to the pharmaceutical or device companies for clinical trials that match its therapeutic area of expertise and patient population. ACRI’s staff has worked closely with world renowned CROs/Sponsors. We are skilled in regulatory functions, community outreach and patient recruitment. We do continuous tracking of clinical studies in pipeline and facilitate study start-up activities. We help with CDAs and feasibility submission, manage clinical studies to promote compliance with ICH/FDA guidelines and ensure safety of subjects. We have experience with CRFs, developing SOPs, managing sponsor audits and monitoring visits. We have working knowledge with different IVRS, EDC, IRB systems
Services provided by ACRI, LLC
➢Bring new study opportunities for Physicians and clinical research sites
➢Keep close follow up with major pharmaceutical companies and CROs in the US and beyond for potential trials.
➢Continue monitoring industry news, chatting with contacts/sponsors/CROs regarding studies they need sites for and what’s in their pipeline. Adding site to the databases of sponsors and CROs.
➢Assist submitting CDAs and Feasibility and follow up with sponsor/CRO until site’s selection status.
➢Evaluate study synopsis to determine enrollment/retention potential and office capacity/capabilities and shortlist suitable phase II, III and IV trials for respective sites and physicians.
➢Provide QA services.
➢Negotiate budget and contract with sponsor.
➢Prepare source documents.
➢Assist with Staff training (GCP, NIH, IATA).
➢Unlimited phone consultations.
➢Provide guidance how to handle SIVs.
➢Hands-on support in business development and regulatory functions.
➢Assist in the development of SOPs and other site wide documentation related to clinical research processes.