It is hard to overestimate the role of the Project Manager to the success of every clinical trial. SynRG Project Managers have a lot of experience and are accredited ACRP members.

Their collaborative approach combined with outstanding organizational and interpersonal skills creates a responsive client-driven environment.

SynRG Project Managers will work in close cooperation with the scientific team to keep you formed on the progress of your clinical trial. They will carefully manage all critical aspects of the study to ensure the delivery of results strictly according to the project timelines.

Our project managers make your project run smoothly, on time, and on budget with a high-quality output.

SynRG Project Management services include:

• Regulatory document package design and submission;
• Ongoing interaction with regulatory authorities and IRBs;
• Investigator site selection and evaluation;
• Investigator meeting organization and site initiation training;
• Budget preparation, negotiation and payment;
• CRA coaching and co-monitoring support;
• Monitoring report review;
• SAE reporting coordination.