Clinical Study Monitoring

Efficient Solutions to Resource-Intensive Study Monitoring

Study monitoring is a resource intensive proposition. Finding, training and managing the CRAs needed to effectively monitor clinical studies to maintain compliance is both time consuming and expensive, especially when hiring these types of professionals into your organization.

We will work with your clinical leads to scope a right-sized solution for your clinical study by ensuring appropriate resources are effectively deployed, to maintain compliance and data integrity.

Our accredited team of monitors have a deep knowledge of clinical studies and the mandatory regulations to ensure your success.

We view our monitors as part of your clinical team, giving your sites a seamlessly integrated impression of your organization.

AlvaMed’s accomplished monitors integrate with your organization to provide the support needed.

Our clients are happy to be references – we are happy to share their contact information when you meet with us.

Ready To Schedule A Call?

We look forward to discussing AlvaMed’s services with you.

Clinical Study Monitoring FAQ's

While many of our clients choose to utilize our full suite of CRO services, we do offer stand-alone Clinical Monitoring.

Yes. Our monitors have experience both on site and working through remote access to satisfy the needs of your monitoring plan.

Our monitors have accreditations from SOCRA, CCRA, and others agencies.

Marc Quartulli

Vice President, Clinical Affairs

At AlvaMed we have a deep pool of CRAs, with extensive knowledge of clinical trials and therapeutic area expertise. We can help you outsource this expensive endeavor, saving you time, cash-burn and headcount expenses, all while delivering highly skilled, experienced clinical professionals, who can integrate seamlessly into your organization, like they were one of your own.

Schedule a meeting with Marc to discuss how AlvaMed can help with clinical study monitoring.