Reference Number: JO-2106-471306_4
Clinical Evaluation Specialist
Rate: £45,000
Job Type: Permanent
Location: Cardiff

Clinical Evaluation Specialist
Medical Device Company
Suitable Locations: Bath, Bristol, Gloucester, Swindon, Cardiff
Salary: Up to 45,000
Benefits: 2-3 days’ home working, 9% pension, private healthcare, annual pay review, bonus

An exciting opportunity has arisen for a Clinical Evaluation Specialist to join an innovative, global medical device company.

We are looking for a Clinical Evaluation Specialist who will be responsible for creating and maintaining Clinical Evaluation Reports for medical device regulatory compliance.

Key Tasks:

– Work alongside the Clinical Operations team and CRO to contribute to Clinical Protocols, data analysis, Clinical Study Report review, and handling any issues arising during the trial (such as device deficiencies and SAEs) within the company.
– Support design control process in areas such as risk, labelling review and clinical data.
– Coordination of Clinical Evaluation using literature review, PMS, PMCF, pre-clinical and clinical data
– Creation of the Clinical Evaluation Report, and update to it during the product lifecycle (e.g. update to literature search or when new Clinical data exists).
– Cross-functional collaboration with Marketing, Regulatory and Legal teams

Experience Required:

– Life Science Degree
– Previous experience in the medical device sector
– Experience of gathering, evaluating and critically interpreting information.
– Experience of creating clear and concise technical documentation.
– Significant experience in critical appraisal, literature review, and/or data analysis

This is a permanent role with a respected global business. As well as a competitive salary and benefits, you will work with an innovative and progressive company that value their employees. If this role is of interest, please send your CV to George.Danchie@cpl.com or call 01189594990 for more information
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