Service 01 / 06
Clinical Trial Management
Full-service study delivery from feasibility through close-out.
Overview
We run Phase I–IV studies end to end, or step into a single function where you already have capacity. Dedicated project teams own timeline, budget and quality from the first feasibility call to the final study report, with risk-based monitoring calibrated to each protocol rather than a fixed visit calendar.
- Risk-based monitoring with dedicated project teams
- Site identification and qualification
- Transparent timeline, budget and enrolment reporting
Capabilities
What this covers.
Each capability can be contracted on its own or as part of the full service line.
- 01
Clinical Trial Feasibility
Protocol assessment, country and site feasibility, realistic enrolment modelling and competitive landscape review — so commitments made to your programme team are achievable.
- 02
Study Start-Up
Regulatory and ethics submissions, site contracting and budgets, essential document collection, and site initiation — managed against a start-up critical path with weekly visibility.
- 03
Clinical Monitoring & Oversight
On-site, remote and centralised monitoring under a risk-based plan, with source data verification scaled to protocol criticality and monitoring visit reports issued on a defined turnaround.
- 04
Project Management
A single accountable project manager, integrated timeline and budget tracking, risk registers, and structured sponsor governance meetings with agreed escalation paths.
- 05
Patient Recruitment Support
Recruitment strategy grounded in real site catchment data, community and referral outreach, ethics-approved participant materials, and retention planning from first-patient-in.
- 06
Site Management
Day-to-day site liaison, training, supply and query management, and performance tracking that surfaces underperforming sites early enough to act on.
Deliverables
What you receive.
Concrete artefacts on an agreed schedule — so progress is verifiable rather than asserted.
- Feasibility report with site and enrolment projections
- Integrated study timeline and budget
- Risk-based monitoring plan
- Monitoring visit reports and follow-up letters
- Enrolment and site performance dashboards
- Trial master file, maintained inspection-ready
- End-of-study close-out documentation
Related services
Often engaged alongside this.
Next step
Scope a clinical trial management engagement.
Share your protocol synopsis and target timeline. We come back with scope, assumptions and an indicative budget.