Senior Clinical Field Specialist

JR United Kingdom; Exeter; On-site; GBP 40,000 - 65,000; Full time

Job summary

A leading company is seeking a Senior Clinical Field Specialist in Exeter to oversee clinical activities for a novel medical device. The role involves managing clinical trials, training staff, and ensuring compliance with regulatory standards. Ideal candidates will have a Bachelor's degree in a relevant field and experience in clinical research.

Qualifications

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

Responsibilities

• Train study staff and supervise setup for quality data collection.
• Manage clinical trial activities from initiation to close-out.
• Collaborate with investigators to ensure data integrity.

Skills

Organizational Skills

Communication Skills

Education

Bachelor’s degree in a relevant health or science field

Master’s degree preferred

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Exeter

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Client:

The Mullings Group

Location:

Exeter, 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 clinical activities for this novel technology, manage clinical trials, and take on advanced proctoring responsibilities.

Responsibilities:

• Train study staff on the correct use of the study device.
• Supervise setup of site workflow to ensure quality data collection.
• Maintain detailed records and documentation.
• Support site staff during live cases.
• Authorize clinical sites for independent use of the device.
• Join clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out.
• Train staff on study procedures and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Collaborate with investigators, site staff, and CROs to ensure data integrity and issue resolution.

Regulatory Support:

• Assist in IRB submissions and audit preparations.
• Ensure compliance with regulatory standards during audits and inspections.

Data Management:

• Ensure accurate data collection and resolve discrepancies.
• Collaborate with Data Management team.

Qualifications:

• Bachelor’s degree in a relevant health or science field; Master’s preferred.
• Experience as a Clinical Research Associate, Clinical Specialist, or similar role.
• 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.