Senior Medical Device Consultant

Pop Science; City Of London; On-site; GBP 70,000 - 90,000; Part time

Job summary

A medical consultancy in the UK is seeking a Senior Clinical Medical Device Consultant. The role involves conducting regulatory strategies for clinical trial activities and collaborating with client teams. The ideal candidate has over 10 years of experience in medical device clinical trials and strong knowledge of EU/UK MDR regulations. Excellent communication skills are essential as you will be reviewing clinical documentation to ensure compliance.

Qualifications

• 10+ years of clinical trial experience for medical devices.
• Proficient in authoring/reviewing clinical trial documentation.
• Detail-oriented with a high level of accuracy.

Responsibilities

• Conduct regulatory strategies for clinical trial activities.
• Collaborate with client teams and review technical files.

Skills

Clinical trial experience for medical devices

Analytical and problem-solving skills

Knowledge of EU/UK MDR regulations

Communication skills

Education

Bachelor’s degree in a relevant discipline

Job description

Senior Clinical Medical Device Consultant

We are seeking a freelance Senior Clinical Medical Device Consultant who has experience conducting regulatory strategies for clinical trial start‑up activities in a variety of European countries, including the UK and Germany. The candidate should also be experienced with authoring and reviewing clinical documentation to ensure compliance with EU/UK regulations and standards. The Senior Clinical Medical Device Consultant will collaborate with client teams and review technical files.

Qualifications

• Bachelor’s degree in a relevant discipline
• 10+ years of clinical trial experience for medical devices, with a proven track record of successful EU MDR study submissions and bringing devices to the EU/UK.
• Strong analytical and problem‑solving skills, with the ability to assess complex regulatory requirements and develop appropriate strategies.
• Strong knowledge of EU/UK MDR regulations.
• Proficient in authoring/reviewing clinical trial documentation for medical devices.
• Excellent written and verbal communication skills, with the ability to effectively communicate regulatory requirements and recommendations to cross‑functional teams.
• Detail‑oriented with a high level of accuracy in regulatory documentation and submissions.
• Ability to work independently and collaboratively, managing multiple projects and priorities simultaneously.
• Excellent written and verbal communication in English.

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