Our LinkedIn survey two months ago showed: Almost half of participants see coordination andorganization as the biggest bottleneck. We have now extended the survey through the end of 2025 – the results confirm the trend:
Coordination and Organization Remain the No. 1 Bottleneck
Study sites today face increasing complexity: multilayered processes, more demanding protocols, more interfaces between teams, trial sites, sponsors, and regulatory bodies. Compliance is mandatory, not optional. Efficient coordination of teams and tasks not only ensures study success but also protects competitiveness and reputation
⛔️ When coordination is lacking – the consequences are noticeable:
For trial sites:
Overworked staff, study delays, or dropouts
Quality risks in data and documentation
High administrative burden
Loss of attractiveness for sponsors
For CROs & sponsors:
Delays in study progress & recruitment
Higher risk of regulatory violations
Increased coordination needs and extra costs
Dependence on the performance of the sites
✅ Keeping studies on track even during bottlenecks
At Camovis, we know that bottlenecks, unclear processes, or missing staff should never slow down study progress. For many years, we have supported trial sites in overcoming these challenges efficiently and pragmatically. Our experienced Clinical Research Professionals temporarily fill staffing gaps, bring structure to complex workflows, and ensure studies continue smoothly – helping to prevent delays, quality risks, or additional costs.
We offer training, consulting, and study-site & DCT solutions to strategically strengthen trial sites and sustainably prepare them for the demands of clinical research.
Efficient coordination is now the decisive success factor – WE ARE AT YOUR SITE