Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist to oversee and manage clinical trials for an innovative medical device designed to enhance heart attack treatment. This role includes training staff, ensuring compliance, and maintaining data integrity during trials across Europe.

Qualifications

• Bachelor’s or master’s degree preferred.
• Experience as Clinical Research Associate or similar required.
• Knowledge of GCP, ISO14155, ICH guidelines essential.

Responsibilities

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

Skills

Organizational skills

Communication skills

Proctoring

Education

Bachelor’s degree in a relevant field

Master’s degree

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, chesterfield

Client:

The Mullings Group

Location:

Chesterfield, United Kingdom

Job Category:

Other

EU work permit required: Yes

Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025

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 for this novel technology, taking 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 proctoring records.
• Support site staff during live cases.
• Authorize clinical sites for independent device use.
• Join clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out, in collaboration with the CPM.
• Train site staff on study procedures and regulatory requirements.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs to resolve issues.

Regulatory Requirements Support:

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

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

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