We are seeking an experienced Medical Writer to lead the development of Clinical Evaluation Reports (CERs) in support of regulatory submissions for orthopaedic devices and technologies.
Key Responsibilities
* Develop high-quality scientific and regulatory content for orthopaedic devices and technologies.
* Lead the creation of Clinical Evaluation Reports (CERs) to support regulatory submissions.
* Collaborate with cross-functional teams to ensure alignment with business objectives.
Requirements
* Masters degree in a relevant field, such as medicine, science or communications.
* At least 5 years of experience in medical writing, preferably in the orthopaedic industry.
* Strong understanding of regulatory requirements for medical devices.
* Excellent communication and project management skills.
Benefits
This role offers a unique opportunity to work on high-profile projects and contribute to the growth of our business. You will have the chance to develop your skills and expertise in medical writing and collaborate with a talented team of professionals.
As a valued member of our team, you can expect a competitive salary package, comprehensive benefits and opportunities for professional development.