We welcome phase II–III clinical studies involving patients with a specific medical condition at Cytokine network centres. We assess the protocol, suggest suitable centres and coordinate their work, from site preparation and recruitment through to study completion.
We review the protocol, eligibility criteria, visit schedule and equipment requirements. Together with investigators, we assess recruitment potential and team capacity. We complete the feasibility questionnaire and suggest suitable centres.
We agree the budget and contract and prepare the documents, facilities, equipment and team. We coordinate submissions to the ethics committee and preparation for the site initiation visit.
We coordinate recruitment through investigators and referral centres. A doctor checks eligibility against the protocol. A coordinator arranges participant visits and examinations.
We maintain site documentation and complete case report forms within our delegated responsibilities. We respond to data queries and report adverse events in accordance with applicable procedures.
We arrange biological sample collection, processing, storage and shipment according to the protocol. We prepare documents and workspace for monitors, help resolve findings and support site close-out.
These timelines are planning estimates and are confirmed for each protocol. Start-up requires the necessary authorisations and approvals, with documents, study drug and centres ready. Ethics committee review follows the committee's own procedures. Recruitment timelines run from site activation. Participant follow-up follows the protocol; data management and monitoring run in parallel.
Preliminary monthly recruitment estimates across the network.
These estimates cover the whole network. Recruitment feasibility for each condition and protocol is confirmed separately, taking account of eligibility criteria, competing studies and site resources.
Investigators, coordinators and site data specialists.
The project coordinator keeps in touch with the sponsor, CRO and centre staff, gathers information on study readiness, coordinates practical arrangements and follows up on agreed actions.
Investigators assess patients against the protocol eligibility criteria, make medical decisions and oversee participant safety. Coordinators help plan visits and procedures, maintain documents and prepare for monitoring visits.
Staff maintain source documents, the investigator site file and case report forms within their delegated responsibilities. They check records for completeness and respond to data queries in a timely manner.
Before the study starts, we define staff responsibilities and the training needed for the protocol, procedures and Good Clinical Practice (GCP). Education, qualification and experience records are reviewed when the team is assembled.
Own and partner centres in the network.
Medical consultations and outpatient procedures on Latyshskikh Strelkov Street. The centre is part of the Cytokine clinical research network.
A partner clinic in the network with its own investigators, equipment and patients. Together with the clinic team, we assess suitability against the protocol requirements. Medical services, doctors and consultation fees are available on the UZI4D website.
Centre website ↗Site participation is agreed based on the study protocol. Visit the centre website to book a medical appointment or find information about services.
Centre website ↗Многопрофильный центр в районе м. Девяткино, работает с 2005 года, создан врачами Военно-медицинской академии. Врачи высшей категории, экспертная УЗ-диагностика, прием по направлениям терапии, урологии, гинекологии и неврологии.
Centre website ↗Is your clinic ready for clinical research? In the Cytokine network we bring studies from sponsors and CROs and support you with documents, site start-up and protocol work. Tell us about your clinic and we will discuss which studies fit.
Apply to joinSend us a protocol synopsis or site feasibility questionnaire. For an initial discussion, please share the therapeutic area, phase, main eligibility criteria and planned timelines.
A single coordinator handles organisational matters. A study agreement is signed with each participating clinic.
Our estimate covers screening, visits, procedures, team time, sample processing and documentation. Following our assessment, we provide a cost breakdown, scope of work and payment terms.
We agree arrangements for sharing confidential materials separately.
We will assess recruitment potential, suggest centres and prepare a cost estimate.
