Junior Clinical Evaluator CV-Library Junior Clinical Evaluator

Scienceabode; Wokingham; On-site; GBP 30,000 - 35,000; Full time

Job summary

A UK medical device manufacturing company is seeking a Junior Clinical Evaluator to assist in the creation and maintenance of Clinical Evaluation Plans and Reports. The successful candidate will conduct research in the respiratory medical device sector, organize technical literature, and manage team administration tasks. This role requires strong data analysis skills, good communication, and the ability to multitask. Experience in the respiratory medical device industry and knowledge of ISO 14971 is advantageous.

Qualifications

• Experience in developing and maintaining Clinical Evaluation Plans and Reports would be an advantage.
• Knowledge of ISO 14971 Risk Management process preferred.
• Experience in the respiratory medical device industry would be advantageous.

Responsibilities

• Assist in the creation and maintenance of Clinical Evaluation Plans/Reports.
• Research recent developments in the respiratory medical device sector.
• Assist with the organisation, evaluation and filing of technical literature.
• Assist with purchasing of publication for the Clinical Evaluation team.
• Administration of the team including organising webinars and events.

Skills

Data analysis

Good communication

Able to work to deadlines

Able to multitask and prioritise workload

Job description

Junior Clinical Evaluator

Location: Head Office (Wokingham UK)
Department: Design and Development
Salary: £30,000 – £35,000
Hours: 40
Contract Type: Permanent

We are looking to recruit a Junior Clinical Evaluator who will assist in creating and maintaining Clinical Evaluation Plans and Reports in compliance with relevant standards and regulations for medical device regulatory approval.

The successful candidate will join our thriving UK medical device manufacturing company and work within our Design & Development Department.

Key Responsibilities

• Assist in the creation and maintenance of Clinical Evaluation Plans/Reports, including development projects according to MEDDEV 2.7.1, Rev. 4 and compliant to EU/UK MDR.
• Research recent developments in the respiratory medical device sector and produce monthly clinical reports.
• Assist with the organisation, evaluation and filing of technical literature, research papers and information into the Technical Literature Library and appropriate Medical Device family group databases.
• Assist with purchasing of publication for the Clinical Evaluation team and other departments.
• Administration of the team like organising webinars, taking care of credit card purchases and organising team events.
• Perform any other duties required by the company.

Desirable Experience / Qualifications

• Experience in developing and maintaining Clinical Evaluation Plans and Reports would be an advantage.
• Knowledge of ISO 14971 Risk Management process preferred.
• Experience in the respiratory medical device industry would be advantageous.

Key Skills

• Data analysis
• Good communication
• Able to work to deadlines
• Able to multitask and prioritise workload