Senior Clinical Field Specialist

JR United Kingdom; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading company is seeking a Senior Clinical Field Specialist to oversee clinical trials for a first-in-class medical device that enhances heart attack treatment. Responsibilities include training staff, managing trial activities, ensuring compliance, and providing regulatory support. The ideal candidate has a relevant degree and experience in clinical research, with strong organizational and communication skills.

Qualifications

• Experience in clinical research, preferably in medical devices or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.

Responsibilities

• Train study staff on the correct use of the study device.
• Manage clinical trial activities from start to finish.
• Conduct site visits to ensure compliance and data integrity.

Skills

Organizational skills

Communication skills

Education

Bachelor’s degree in a relevant field

Master’s degree (preferred)

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, London

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Client:

The Mullings Group

Location:

London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025

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Job Description:

In recent decades, treatment of heart attacks by minimally invasive percutaneous coronary intervention (PCI) has significantly improved patient outcomes. However, successful re-opening of narrow or blocked coronary arteries does not always restore blood flow to the entire heart muscle.

Our client is developing a first-in-class medical device that will diagnose MVO in real-time during PCI and serve as a treatment platform in the cath lab.

As they roll out their clinical trial across Europe, we are hiring a Senior Clinical Research Specialist to oversee and manage clinical trials, support proctoring activities, and take on advanced responsibilities.

Responsibilities:

• Train study staff on the correct use of the study device.
• Support site setup to ensure quality data collection.
• Maintain detailed proctoring records.
• Assist during live cases to ensure safety and efficacy.
• Authorize sites for independent device use.
• Join clinical cases for support.
• Manage clinical trial activities from start to finish.
• Train staff on study procedures and regulatory requirements.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs.

Regulatory Support:

• Assist with IRB submissions and audits.
• Ensure compliance with regulations.

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in a relevant field; master’s preferred.
• Experience in clinical research, preferably in medical devices or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency with CTMS and EDC software.