For sites & investigators
Research built on documentation, not just enrolment.
Sites that enrol quickly and document poorly cost sponsors more than they deliver. We select and develop investigators against both — and invest in the second, because it is the part that can be taught.
What we provide
Support that makes participation workable.
Running a trial alongside a clinical service is demanding. These are the things we take off the site's plate.
GCP training and refreshers
ICH-GCP training for the full site team, with documented completion records maintained in the site file.
Start-up handled for you
We prepare regulatory and ethics submissions, assemble essential documents and manage contracting so your team can focus on patients.
A monitor who knows the protocol
Consistent CRA assignment rather than a rotating roster, with queries answered on a defined turnaround.
Recruitment support
Ethics-approved participant materials, referral pathway development and community outreach where the protocol allows.
Timely payments
Milestone-based site payments processed to an agreed schedule, with transparent reconciliation.
Research capacity building
Sites that perform well are brought into successive studies, building durable research capability rather than one-off participation.
Qualification
What we look for in a site.
Not every criterion has to be met on day one — several can be developed with our support. Tell us where you stand and we will be straight about the gap.
- A qualified principal investigator with relevant specialty experience
- Access to the target patient population in sufficient volume
- A dedicated study coordinator, or willingness to appoint one
- Adequate facilities for study procedures and investigational product storage
- Institutional ethics committee access, or willingness to work through the NBC
- Commitment to source documentation standards and query turnaround
Already running research at your institution? Send your site profile, specialty and approximate patient volumes to contact@clinertia.com and we will come back with the studies you may be a fit for.
Investigators
Tell us about your site.
Specialty, patient volumes, facilities and prior research experience — that is enough for a first conversation about which studies you could join.