Job summary
Job post source
This job is directly from Cordis
Job overview
The Clinical Research Associate (Coronary) at Cordis plays a crucial role in supporting the coronary program by ensuring FDA clearance through PMA approval for innovative coronary devices, directly impacting patient access and care.
Responsibilities and impact
The role involves supervising study sites, managing Trial Master Files, organizing Steering Committee events, preparing reports and dashboards, coordinating with CRO and Core Labs, assisting with meetings and audits, and ensuring compliance with study protocols and regulations.
Compensation and benefits
The position offers a pre-tax salary range of $66,000 to $82,500 annually, with pay varying based on skills, education, experience, and location. US work authorization is required, and Cordis emphasizes equal opportunity employment with inclusive workplace values.
Experience and skills
Candidates need 3-5 years of medical device experience in CRO or Sponsor settings with knowledge of ICH and GCP guidelines, a Bachelor's degree, and preferred experience in IDE clinical studies and coronary/cardiac clinical studies. Strong communication, attention to detail, independence, and ability to work across time zones are essential.
Work environment and culture
Cordis promotes a diverse and inclusive work environment valuing different backgrounds, experiences, and perspectives, fostering equity and inclusion as core responsibilities of all teammates.
Company information
Cordis partners with Selution to develop advanced drug device combination products targeting coronary and peripheral artery disease, aiming to revolutionize healthcare with next-generation medical solutions.
Job location and travel
This is a remote position with responsibilities that may require coordination across multiple time zones including Europe.
Unique job features
The role offers the unique opportunity to contribute to a high-priority, multi-center IDE clinical trial in the coronary space, directly influencing the success of innovative medical devices and patient care improvements.
Company overview
Cordis is a global leader in the development and manufacturing of interventional vascular technology. They specialize in cardiovascular and endovascular products, including stents, catheters, and guidewires, which are essential for minimally invasive procedures. Founded in 1959, Cordis has a rich history of innovation and was a pioneer in the development of balloon angioplasty. The company generates revenue through the sale of its medical devices to hospitals and healthcare providers worldwide, focusing on improving patient outcomes and advancing medical technology.
How to land this job
Position your resume to highlight your experience with clinical trials, especially in the medical device space and familiarity with ICH and GCP guidelines, as these are critical for the Clinical Research Associate role at Cordis.
Emphasize skills in site management, trial master file maintenance, and your ability to work independently across multiple time zones, including coordination with global teams.
Apply through multiple platforms such as Cordis' official corporate career site, LinkedIn, and other job boards where the position is posted to maximize your application visibility.
Connect on LinkedIn with current employees in Cordis' coronary or clinical research divisions; start conversations by referencing recent Cordis innovations in coronary devices or asking about the team’s approach to IDE clinical trials.
Optimize your resume for ATS by incorporating keywords from the job description like 'clinical trials,' 'ICH,' 'GCP,' 'site management,' 'Trial Master Files,' and 'IDE clinical study' to ensure it passes initial automated screenings.
Use Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application portals, and find relevant LinkedIn contacts, allowing you to focus your energy on preparing for interviews and networking.
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