Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist in Maidstone to oversee clinical trials for a groundbreaking medical device in cardiac care. You will play a vital role in training, managing site operations, and ensuring compliance with regulatory standards, contributing to innovative healthcare solutions.

Qualifications

• Experience as Clinical Research Associate, Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Proven proctoring and site management experience preferred.

Responsibilities

• Train staff on the correct use of the device.
• Manage clinical trial activities from initiation to close-out.
• Ensure compliance with regulatory standards.

Skills

Organizational skills

Communication skills

Interpersonal 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, Maidstone

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Client:

The Mullings Group

Location:

Maidstone, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

12

Posted:

28.06.2025

Expiry Date:

12.08.2025

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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 the clinical activity for this innovative technology, and take on advanced proctoring responsibilities.

Responsibilities:

Proctoring and Case Support Duties:

• Train study staff on the correct use of the device.
• Supervise site workflow setup to ensure quality data collection.
• Maintain detailed records and documentation.
• Support site staff during live cases.
• Authorize sites for independent device use in agreement with CPM.
• Join clinical cases to support device use.

Clinical Trial Support:

• Manage clinical trial activities from initiation to close-out.
• Train staff on study procedures and software.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs.

Regulatory Requirements Support:

• Assist with IRB submissions and audits.
• Ensure compliance with regulatory standards.

Data Management:

• Ensure accurate data collection and resolution of discrepancies.

Qualifications:

• Bachelor’s degree in a relevant field; Master’s preferred.
• Experience as Clinical Research Associate, Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Proven proctoring and site management experience preferred.
• Strong organizational, communication, and interpersonal skills.
• Proficiency in CTMS and EDC software.