Services
Clinical operations help from people who have run studies
We start with your problem, not a fixed product. Then we bring the right people and tools, and stay involved until it is solved.
What we do
Clinical project management
A project manager who builds the plan, runs the timeline and keeps sponsors, CROs and sites on the same page.
Study start-up support
Help with site documents, approvals, budgets and the checklist that gets the first participant enrolled.
Inspection readiness
A review of your trial records, logs and SOPs, with a clear list of what to fix before an audit or inspection.
Study and process review
An honest look at a study, process or program, with practical next steps instead of a generic report.
Clinical data reporting
Clear dashboards that bring study, site and operations data together so your team can act on it.
Vetted clinical talent
Clinical, medical and regulatory professionals matched on experience and working style, for one role or a full team.
How we work
01
Understand
A short call to learn what is slowing your study down.
02
Plan
A written scope with people, timeline and price.
03
Deliver
Senior people do the work and report progress until it is done.
Questions
Do I need Protocol AI to use your services?
No. Our services work on their own or alongside Protocol AI and the systems you already use.
How are services priced?
Services are scoped to your study and quoted in writing before work starts.
Tell us what is slowing your study down
A 30-minute call with our team. You leave with a clear next step, whether or not you work with us.
Prefer email? Write to jmodi@manakiki.net. A person replies, usually within one business day.