Director of Clinical Affairs

CM Medical is partnered with a global medical device manufacturer in the cardiovascular space.

Our client is a fast-growing medical device manufacturer who focus exclusively in cardiology; interventional cardiology and structural heart.

We are looking to recruit a Director of Clinical Affairs/Clinical Operations to join the team to manage and execute the upcoming clinical trials in the US. The role will have a global focus, but to begin with, will be predominantly oriented around the US.

Reporting to the Global Head of Regulatory Affairs, you will be responsible for managing the clinical study and managing clinical sites; approximately 60/70 sites in the US. You will be responsible for KOL interaction and development, managing investigational sites and leveraging KOL relationships.

Our client is the manufacturer of a highly innovative transcatheter device for the Tricuspid valve (TTVR) as well as other structural heart products. As such, we're seeking someone with existing experience in structural heart.

Requirements:

• Be based anywhere in the US (No relocation or Visa support on offer).
• Ideally a minimum of 10 years of experience with class III medical devices
• Experience in managing global clinical trials
• Experience with structural heart devices (TAVR/TMVR/TTVR)
• Willingness to travel (Up to 50%)
• Start-up experience is HIGHLY preferred; Flexibility, ability to work in fast-paced environments, wear multiple hats etc.

We are looking to start the interview and onboarding process ASAP. To be considered, please apply directly or email james.christopher@medical-cm.com to discuss further.

Please note; I anticipate a high volume of applicants and I'm simply unable to respond to all. If you do not meet the above criteria and haven't heard from me within 14 days of applying, please assume your application has been unsuccessful.