Site Coordinators
- Visit scheduling and participant follow-up
- Source documentation and electronic case report form (eCRF) entry support
- Investigator Site File upkeep
- Preparation for monitoring visits and audits
Integrated site support services
Choose a single service or a tailored combination — every engagement is shaped around the site, the protocol and the people involved.
Services / At the site
Capable hands where the study happens
Clinical Study Nurses
- Protocol procedures such as vital signs, sampling and ECGs
- Sample processing and shipment per lab manual
- Attentive observation of participant wellbeing
- Accurate, contemporaneous records
External Site Support
- Extra capacity during start-up or peak workload
- Continuity cover when site staff are absent
- Ethics and regulatory document support
- Query resolution and close-out support
All site-based activities are performed under Principal Investigator oversight and recorded on the study delegation log.
Services / Beyond the site
Specialist support that extends the site’s reach
Home Health Visits
Protocol-defined procedures at the participant’s home — only where protocol, local regulation and participant consent allow, with the same documentation standards as on site.
Direct-to-Patient Logistics
Coordinated delivery of eligible study materials with chain-of-custody records, respecting participant privacy at every handover.
Radiology & Nuclear Medicine
Specialist imaging assessment and reporting support, aligned with the protocol’s imaging requirements.
Pharmacy & Ancillary Supplies
Coordination of study materials and ancillary supplies, with accountability records that support inspection readiness.
Availability of specialist services depends on geography, protocol and local requirements.