Clinical Field Specialist, Selution

Overview

About Us:

Cordis is an independent, customer-focused global provider of interventional cardiovascular medical technologies. During our 60 year history we’ve established a legacy of pioneering breakthrough technologies, including the first guiding catheters and coronary drug eluting stents. Cordis has built a strong global footprint that spans over 70 countries.

We’re teammates, not just employees. Our culture empowers you to act like an owner and unleash your full potential in the process. With diverse teams on a global scale, we foster an inclusive atmosphere where everyone is embraced for who they are, their unique perspective, and what they bring to the table. We believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients.

If you love a challenge and are ready to have a direct, positive impact on the lives of millions, then Cordis is just the place for you. Join us, and let’s improve the wellbeing of millions, together.

We are the people behind the people who keep saving lives.

Clinical Field Specialist (CFS) : position that provides case support to physicians within a given territory. Case support provided on peripheral and coronary interventional procedures in pre-market and post-market phases of product development with SELUTION-SLR. The CFS plays a critical role in clinical studies including device training, case support and ensuring timely data collection for clinical programs.

Responsibilities

• Perform Physician and hospital staff training and procedural case coverage to ensure safe and effective use of the device
• Present clinical study training materials based on investigational plans including study protocol, IFU, core lab manuals and case report forms
• Provide field support for clinical studies by participating in site selection, site initiation and activation, supporting cases, ensuring quality data acquisition throughout follow up and performing study closure activities
• Address clinical research site needs by maintaining frequent contact via email/phone/on-site visits with PI's and research coordinators
• Responsible for gaining and maintaining knowledge of clinical sites in a given geographical area to best understand and assess investigators interests and capabilities
• Manage key study sites (investigators and research staff) and serve as 'live' point of contact with the site for communication with SELUTION CSM, CRA, and CRO team
• Partner with SELUTION clinical research teammates to meet business needs in the field including site CIP questions, re-training, case coverage, data entry/query resolution and escalation of critical issues
• Administrative activities including evaluating metrics, data entry into trackers, documentation of activities and site feedback to SELUTION study teams
• Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines and policies
• Identify and mitigate quality risks and issues for assigned clinical studies with oversight from study management team
• Assist with oversight of activities performed by CRO
• Maintain in-depth knowledge of current study protocols, process and procedures to assist sites and facilitate study management team efforts
  
  
  

Role Expectations:

• Reside within designated geographic territory to facilitate on-site visits to assigned clinical sites
• Be available to cross-cover sites as back up for other CFS territories, including holding necessary credentialing
• Attend and lead SIV and site activation activities at assigned sites (in-person priority) for duration of the event
• Attend start-up phase enrollments and clinical follow up visits at each assigned site to ensure site protocol compliance, image upload and readability and quality data collection
• Prioritize regular communication with study management team and CRO
  
  
  

Qualifications

Bachelor’s Degree in a life science, nursing, engineering, or healthcare related field (preferred)

Minimum Two Years’ Experience With Cardiovascular Procedures

Minimum two years’ experience working directly with physicians and healthcare professionals

Prior Experience With Clinical Trials (preferred)

Experience in coronary and peripheral interventions

Experience with Good Clinical Practice (GDP) and/or regulatory compliance guidelines for clinical studies

Physical Requirements:

Ability to travel (at least 75%) to company and sites

Pay / Compensation

The expected pre-tax pay rate for this position is $73,700 - $100,000 per year

Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.

Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All our teammate’s points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.