01
Clinical project management
- Scope, timeline, and milestone planning
- Cross-functional governance
- Risk, issue, and decision management
- Sponsor and vendor coordination
- Forecast and change visibility
Clinical research services
Flexible support for Phase I–IV trials.
Engage an experienced team for an integrated scope, a defined function, or a hybrid model that evolves as the clinical research program and internal team change.
Discuss your needs02
Study start-up
- Start-up planning and trackers
- Essential-document collection
- ICF and IRB/EC coordination
- Contract and activation dependencies
- Site readiness and training oversight
03
Feasibility & site selection
- Protocol and operational-burden review
- Country and site assumptions
- Enrollment feasibility
- Site capability assessment
- Selection documentation
04
Clinical monitoring
- Monitoring strategy and planning
- Site qualification, initiation, monitoring, and closeout
- Action-item and deviation follow-up
- Site relationship management
- Escalation and trend reporting
05
Site & vendor oversight
- Role and responsibility definition
- Performance and dependency tracking
- Operational issue resolution
- Meeting and escalation cadence
- Sponsor oversight support
06
TMF & inspection readiness
- TMF expectations and ownership
- Document-quality review
- Completeness and timeliness tracking
- Reconciliation planning
- Inspection-readiness support
Engagement models
Choose the level of ownership that fits.
Full-service
Integrated ownership across the functions agreed for a study or clinical research program.
Functional service
Dedicated capability embedded into sponsor governance and systems.
Hybrid / adaptive
Shared ownership with scope and resourcing adjusted as the program evolves.
Discuss your program
Define the right first engagement.
Share your program stage, critical milestones, countries, sites, and the functions requiring ownership or support.