Field Specialist, Clinical Research (Remote/National Travel) at Cordis
Irvine, CA 92618, USA -
Full Time


Start Date

Immediate

Expiry Date

09 Nov, 25

Salary

76450.0

Posted On

10 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research, Cath Lab, Clinical Trials, Life Sciences

Industry

Pharmaceuticals

Description

Overview:
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.
Responsibilities:
The Field Specialist, Clinical Research 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.

QUALIFICATIONS

  • Bachelor’s Degree in life sciences, nursing, engineering, or healthcare related field (preferred)
  • Minimum 3 years’ experience with cardiovascular procedures in clinical research in this same role or as a nurse or tech as radiology tech or Cath lab tech
  • Minimum 3 years’ experience working directly with physicians and healthcare professionals
  • Prior experience with clinical trials (preferred)
  • Experience in coronary or peripheral interventions
  • Ability to travel (at least 75%) to company and clinical trial sites

How To Apply:

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Responsibilities
  • 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:
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