Job Description

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 seeking a motivated and detail-oriented Entry-Level CER Specialist/Medical Writer to join our team. The successful candidate will be responsible for preparing and maintaining Clinical Evaluation Reports (CERs) and other medical writing tasks to support regulatory submissions and product development.

• Assist in the preparation and maintenance of Clinical Evaluation Reports (CERs) in compliance with regulatory requirements.
• Conduct literature searches and reviews to gather relevant clinical data.
• Analyze and interpret clinical data to support CERs and other regulatory documents.
• Collaborate with cross-functional teams, including regulatory affairs, clinical research, and product development.
• Ensure accuracy, clarity, and consistency in all written materials.
• Stay updated with current regulations, guidelines, and industry best practices related to CERs and medical writing.
• Participate in training and development opportunities to enhance skills and knowledge.

• Bachelor’s degree in Life Sciences, Biomedical Engineering, Pharmacy, or a related field.
• Level of work experience in any healthcare setting-0-2 years
• Strong written and verbal communication skills.
• Attention to detail and ability to work independently.
• Basic understanding of clinical research and regulatory requirements.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Ability to manage multiple tasks and meet deadlines.

Preferred Qualifications:

• Previous experience or internship in medical writing or clinical research.
• Familiarity with medical terminology and clinical data analysis.
• Knowledge of regulatory guidelines (e.g., MDR, MEDDEV 2.7/1).

Job Tags

Similar Jobs