Edwards Lifesciences is the global leader in the science of heart valves and hemodynamic monitoring, with more than five decades of experience in partnering with clinicians to develop life-saving innovations. Headquartered in
For us, helping patients is not a slogan – it's our life’s work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we help ensure that patients regain and even improve their quality of life.
Principal Clinical Research Associate (
This is an exciting opportunity within our Critical Care division to advance patient care through clinical research. We are looking for a highly motivated individual to work in our rapidly changing and expanding Critical Care Division. This is a fast paced environment with many studies in progress and planned for the near future.
As a CRA, you will be responsible for field monitoring and also remote data collection within our clinical studies. In addition you will be responsible for the overall day to day management of study sites and be actively involved in protocol and CRF development and the creation of appropriate edit specifications. Day to day activities will include significant travel to our study sites, field monitoring as well as cross functional teamwork with our Regional offices.
Our Requirements:
This position Requires a minimum of six/seven years hands-on clinical research experience, encompassing all aspects of the clinical process, with at least 2 years field monitoring within the medical device industry. A medical/nursing background is preferable. Our CRA team will be expanding with plenty of room for career development in the future.
•A Bachelors degree in a related biological or life sciences discipline required.
•Experience working with Critical Care studies desirable.
•Understanding of cardiovascular anatomy, pathology and physiology with the ability to communicate with various clinical personnel within the Critical Care environment.
•Understanding of medical device regulatory documents/device accountability/adverse event reporting.
•Willing to travel 50% to 75% when necessary.
How to Apply:
At Edwards Lifesciences, we want you to have as much information as possible before making an important career decision. To find out more about this role and the opportunity it offers, please visit our website:
www.edwards.com
OR
To apply directly to this position, please click the link below or cut and paste it into your browser:
http://www.edwards.com/Careers/reqfinder?urlvariablestring=3767
***Note to Agencies and Recruiters: Edwards Lifesciences is not accepting referrals from Agencies or Recruiters.
Resumes received by Edwards Lifesciences from search firms and/or individual recruiters are considered unsolicited.
Agencies and Recruiters: Refrain from contacting managers directly, to solicit job orders. Contact the Edwards Lifesciences Human Resources Department via e-mail at EW_Talent_Acquisition@edwards.com or call our dedicated Talent Acquisition hotline at 949-250-3422. Thank you.
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http://www.edwards.com/Careers/reqfinder?urlvariablestring=3767
Edwards Lifesciences