Clinical Evaluator

Intersurgical

View: 104

Update day: 07-05-2024

Location: Wokingham South East

Category: Education / Training

Industry: Medical Practice

Position: Associate

Job type: Full-time

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Job content

An exciting opportunity has arisen for a Clinical Evaluator to join our thriving UK medical manufacturing company.

We are looking to recruit a Clinical Evaluator who will be responsible for the creation and maintenance of Clinical Evaluation Reports for medical device regulatory compliance.

The successful candidate will be able to complete technical documentation, including literature reviews, with a high degree of accuracy and attention to detail.

Clinical Evaluator Requirements

Essential Experience/Qualifications:

Educated to at least BSc level (or equivalent) in a life science or other relevant scientific subject (e.g. Physics).

Significant experience in critical appraisal, literature review, and/or data analysis (postgraduate study may count towards this experience).

Able to produce clear and concise technical documentation.

Desirable Experience/Qualifications

Previous experience in the medical device industry.

Knowledge and understanding of medical device regulations, in particular the EU MDR regulation and MedDev 2.7.1 rev. 4.

Knowledge of medical statistics.

Key Skills

Good communication.

Able to work to deadlines.

Able to multitask and prioritise workload.

Able to make decisions and self manage.

Able to work in a team and on own initiative.

Self-motivated and willing to learn.

Have a can-do attitude with an enthusiastic approach to work.

I.T. Literate - Microsoft Office.

Medical writing.

Methodical, organised and structured approach to work.

Excellent attention to detail.

Excellent report writing skills.

Able to gather, evaluate, critically interpret and communicate information.

Able to function in a highly regulatory environment with a focus on compliance.

High level of commitment.

Flexibility to work additional hours if required to support the facility.

About Intersurgical

Intersurgical was formed in 1982 in the UK and started with a modest range of respiratory products. Since its inception, the company has continued to grow and develop and today is the respiratory care specialist in airway management, anaesthesia, critical care and oxygen & aerosol therapy.

The company was formed with seven people, producing a limited product range for the UK hospital market. Today, we employ over 3500 people, producing an extensive product range sold worldwide. We operate across five manufacturing sites and have direct sales operations in over 25 countries and a number of export offices located throughout the world supporting our network of speciality distributors.

Through a constant programme of new product and market development Intersurgical is today one of the market leaders for high quality respiratory care products for the hospital sector worldwide.

Our products are seen as easy to use, technically superior and of the highest quality. The product range is innovative and we will continue to develop and implement improvements.

Location: Head Office (Wokingham UK), Berkshire

Type: Full time, Permanent

Hours of Work: 40 hours per week, Monday to Friday

Salary: Competitive

You may have experience of the following: Compliance Assistant, Compliance Administrator, Compliance Administration, Compliance Analyst, Clinical Evaluation, Clinical Research, Life Sciences, Document Controller, Medical Devices, Product Evaluation, Product Tester, Product Testing, Research Analyst, Regulatory Compliance, Regulatory Affairs, Data Analyst, Data Analysis, etc.

Ref: (phone number removed)
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Deadline: 21-06-2024

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