Job summary
Job post source
This job is directly from Cordis
Job overview
The Clinical Research Associate at Cordis is responsible for managing clinical trial sites to ensure accurate data collection and compliance with protocols, contributing to the development of advanced drug device combination products for cardiovascular disease treatment.
Responsibilities and impact
The CRA will initiate, maintain, and close trial sites, ensure compliance with clinical protocols and regulatory requirements, support site training, manage trial data accuracy, drive recruitment and retention strategies, and assist with audit readiness and monitoring activities.
Compensation and benefits
The position offers a pre-tax salary range of $94,600 to $127,600 per year, with actual pay dependent on skills, education, experience, and location. US work authorization is required. Cordis promotes equal opportunity and an inclusive work environment.
Experience and skills
Candidates should have at least 5 years of clinical research associate experience, preferably with onsite monitoring and site management in medical device trials within the cardiovascular space, proficiency in MS Office, and strong interpersonal and negotiation skills. Travel up to 65% is required.
Work environment and culture
Cordis values diversity, equity, and inclusion, fostering a welcoming and supportive environment where teammates bring varied experiences and backgrounds united by a passion for improving lives.
Company information
Cordis specializes in developing and commercializing innovative drug device combination products for coronary and peripheral artery disease, aiming to revolutionize healthcare with next-generation solutions.
Job location and travel
This is a remote position with travel requirements of approximately 65% to meet trial milestones.
Unique job features
The role involves working on cutting-edge cardiovascular medical device trials, contributing directly to improving patient care and supporting regulatory submissions such as PMA and IDE trials.
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 clinical research experience, especially in medical device trials and cardiovascular studies, as this aligns directly with Cordis' focus on advanced drug device combination products.
Emphasize your skills in site management, monitoring, regulatory compliance (ICH-GCP, ISO 14155), and your ability to handle trial initiation, maintenance, and closure effectively.
Apply through multiple platforms including the Cordis corporate careers site, LinkedIn, and relevant clinical research job boards to maximize your application reach.
Connect with clinical team members or current Clinical Research Associates at Cordis on LinkedIn; use ice breakers like commenting on Cordis’ recent innovations in cardiovascular treatments or asking about their experience managing trial sites remotely.
Optimize your resume for ATS by incorporating keywords such as 'clinical monitoring,' 'site management,' 'ICH-GCP,' 'ISO 14155,' 'trial initiation,' and 'device accountability' to ensure it passes automated screenings.
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