Clinical Trial Recruitment and Treatment

The key to a successful trial is high quality Project Management. Our people understand the commitment and dedication required to deliver study objectives in a timely and cost efficient manner. In the battle to win your business many CROs provide overly optimistic timelines and underestimated budgets, leading to a failure to deliver on time and requests for extra payments. At Crionna we believe such tactics to be counter productive; we prefer long term relationships with our clients based on trust. We take care when preparing timelines and study budgets to ensure that they are realistic and as cost efficient as possible.

The Project Manager plays the pivotal role in the communication flow between sponsor, CRA and Investigator to ensure that studies are performed and monitored to the exacting standards required by the FDA and EMEA. Our CRAs perform diligent and thorough study monitoring to ensure fast turnaround of data collection. The Project Manager ensures close communication with our Pharmacovigilance and Medical Monitoring team to ensure good SAE resolution and timely reporting to the competent authorities. If, despite good planning, recruitment is slow Crionna has an armament of recruitment strategies to address the problem.