Job summary
Job post source
This job is directly from Cordis
Job overview
The Sr. Clinical Research Associate at Cordis plays a critical role in supporting clinical trials for innovative coronary devices, contributing to FDA approval and patient access to new treatments.
Responsibilities and impact
The role involves supervising study sites, managing Trial Master Files, coordinating Steering Committee events, preparing reports, collaborating with CRO and Core Labs, ensuring study compliance, assisting with audits, and managing site communications.
Compensation and benefits
The position offers a salary range of $94,600 to $127,600 annually, with pay varying by experience and location; US work authorization is required, and Cordis promotes equal opportunity employment.
Experience and skills
Candidates need a bachelor's degree and 5+ years in medical device clinical research under ICH and GCP guidelines; preferred skills include attention to detail, effective communication, independence, time management, and ability to work across multiple time zones.
Work environment and culture
Cordis values diversity, inclusion, and equity, fostering a welcoming environment where different backgrounds and perspectives contribute to success.
Company information
Cordis, in partnership with Selution, develops advanced drug-device combination products targeting coronary and peripheral artery disease with a mission to revolutionize healthcare.
Job location and travel
This is a remote position with potential coordination across multiple time zones including Europe.
Unique job features
The role offers the unique opportunity to be directly involved in a pivotal clinical trial for a groundbreaking coronary device, impacting patient care and regulatory approval.
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
Tailor your resume to highlight your extensive experience in managing clinical trials within the medical device space, emphasizing your knowledge of ICH and GCP guidelines and your ability to supervise multi-center studies effectively.
Focus on showcasing your skills in regulatory compliance, Trial Master File management, and coordination with CROs and Core Labs, as these are critical for ensuring FDA clearance and study success at Cordis.
Apply through multiple platforms including the Cordis corporate career site and LinkedIn to maximize your chances of your application being noticed for the Sr. Clinical Research Associate position.
Connect with current clinical research professionals at Cordis on LinkedIn, particularly those in the coronary or clinical operations divisions, using ice breakers such as commenting on recent Cordis clinical trial advancements or asking about their experience working on IDE trials.
Optimize your resume for ATS by incorporating keywords from the job description like 'clinical trial management,' 'ICH guidelines,' 'GCP compliance,' 'Trial Master File,' and 'FDA clearance' to improve your chances of passing initial automated screenings.
Use Jennie Johnson's Power Apply feature to automate the application process across multiple job boards and LinkedIn, tailor your resume with relevant keywords, and identify key Cordis contacts to network with, allowing you to focus your time on preparing for interviews and follow-ups.
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