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Details

Medical Advisor (Medical Devices)


Reference:KS/AKEQ-202663 Location: Limerick
Qualification:DegreeExperience:1-2 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Doctor (Medical), Medical Advisor

Our client is a leading Medical Device organisation based in Limerick. They are seeking a Medical Doctor with strong interpersonal skills to collaborate across business functions and business units, applying clinical knowledge and expertise to support device benefit and risk assessment, regulatory submissions, product development, internal and external training, market research, and sales and marketing efforts.

Role/Responsibilities:
• Build and maintain a working knowledge of product lines, both new and existing products, and the clinical procedures in which they are used. Have a clinical understanding of the risks, benefits, and patient selection & treatment options for the appropriate disease groups.
• Work closely with Quality Assurance, Engineering, and Regulatory functions to understand and document state of the art, conduct risk analyses, health risk assessments, and risk-benefit determinations of the medical devices throughout their life cycles.
• Provide essential medical judgment in the review and risk assessment of product complaints, post-market quality issues, Health Risk Assessments and Health Hazard Analysis.
• Represent the voice of the clinicians and other health care workers to Research and Development teams as required. Keep abreast of the latest developments & clinical best practices in the clinical areas of interest to the organisation.
• Provide critical clinical review of our clients documents that will be seen by internal and/or external customers, including Instructions for use for the devices, marketing and promotional pieces, training and educational materials, and press releases.
• Foster relationships with and establish a pool of physicians who can provide clinical expertise and input to specific projects within the Regulatory, Quality, Engineering or Marketing functions as required.
• Provide clinical input and review of the post market surveillance process and required reports and documentation.
• Work with cross-functional teams in the pre-market and post-market settings to identify gaps in the clinical evidence for our clients products and provide clinical input required to fill those gaps, including contributing to clinical trial design, reviewing/approving Clinical Evaluation Reports, and reviewing/approving risk-benefit analyses.
• Develop and manage relationships with clinical key opinion leaders
• Provide clinical experience and support to Regulatory Affairs, Engineering, Marketing, Quality Assurance, and other internal groups as needed.
• Participate in audits by external bodies to provide clinical input.

Education/Experience:
• Medical Degree MD or recognised equivalent (residency training/practice experience preferred but not essential).
• Strong technical writing and analytical skills
• Interest and skilled at literature- and web-based research
• Strong interpersonal skills and the ability to communicate at all levels of the organisation.
• Proven problem-solving skills.
• Good computer skills including knowledge of Microsoft® Office.
• Excellent organisational skills.
• High self-motivation.
• Willingness and availability to travel on company business.


If you would like further Information you can contact the recruiter directly:

Karen Shiel | Tel: +353 (0) 1 5079256