Senior Clinical Field Specialist

JR United Kingdom; Dartford; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading company in medical innovation is seeking a Senior Clinical Field Specialist in Dartford. You will oversee clinical trials for an innovative heart treatment device, focusing on training and proctoring staff, regulatory compliance, and data management. This role requires a background in health sciences and significant experience in clinical research.

Qualifications

• Experience as Clinical Research Associate, Specialist, or in similar roles.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Experience in proctoring and site management preferred.

Responsibilities

• Train study staff on the correct use of the study device.
• Manage clinical trial activities from initiation to close-out.
• Assist with IRB submissions and ensure compliance with regulatory standards.

Skills

Organizational skills

Communication skills

Proctoring

Education

Bachelor’s degree in a relevant health science field

Master’s preferred

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, dartford

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Client:

The Mullings Group

Location:

dartford, 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 myocardial microvascular obstruction (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 for this innovative technology, including advanced proctoring responsibilities.

Responsibilities:

Proctoring and Case Support Duties

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

Clinical Trial Support

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

Regulatory Requirements Support

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

Data Management

• Ensure accurate data collection and resolve discrepancies.
• Work with Data Management team for data integrity.

Qualifications:

• Bachelor’s degree in a relevant health science field; master’s preferred.
• Experience as Clinical Research Associate, Specialist, or similar in medical devices or CROs.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency in CTMS and EDC software.