Freelance EU MDR Regulatory Lead for Medical Devices

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

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.