Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist to drive clinical activity for an innovative medical device. This role involves training site staff, managing clinical trials, and ensuring compliance with regulatory requirements. Candidates should have a degree in life sciences and relevant experience in clinical research.

Qualifications

• Experience as Clinical Research Associate or Clinical Specialist.
• 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.
• Supervise site workflow to ensure quality data collection.
• Manage clinical trial activities from initiation to close-out.

Skills

Organization

Communication

Independence

Teamwork

Education

Bachelor’s degree in life sciences

Master’s degree in life sciences

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Manchester

Client: The Mullings Group

Location: Manchester, United Kingdom

Job Category: Other

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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 help drive clinical activity for their innovative technology, oversee and manage clinical trials, and take on advanced proctoring responsibilities.

Responsibilities:

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

Regulatory Requirements Support:

• Assist in IRB submissions and documentation.
• Support audits and inspections, ensuring compliance.

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in life sciences or healthcare; master’s preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulations.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Ability to work independently and in teams.
• Proficiency in CTMS and EDC software.