Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist to oversee clinical trials for a groundbreaking medical device in Cardiff. This role includes training staff, managing site activities, and ensuring regulatory compliance, making it ideal for those with clinical research experience looking to contribute to innovative healthcare solutions.

Qualifications

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

Responsibilities

• Manage clinical trial activities from initiation to close-out.
• Train staff on study procedures and ensure compliance.
• Supervise proctoring and case support duties.

Skills

Organizational skills

Communication skills

Interpersonal skills

Ability to work independently

Collaborative skills

Education

Bachelor’s degree in a relevant field

Master’s preferred

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Cardiff

Client: The Mullings Group

Location: Cardiff, 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, support the use of the novel 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 for consistent image and measurement collection.
• Maintain detailed proctoring records.
• Support site staff during live cases.
• Authorize sites for independent device use in agreement with CPM.
• Join clinical cases to ensure safe device use.

• Clinical Trial Support:
• Manage activities from study initiation to close-out.
• Train staff on study procedures, software, and regulatory requirements.
• Conduct site visits for qualification, initiation, monitoring, and close-out.
• Collaborate with investigators and CROs for issue resolution and data integrity.

• Regulatory Requirements Support:
• Assist with IRB submissions and audits.

• Data Management:
• Ensure accurate data collection and collaborate with Data Management to 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, and regulatory standards.
• Experience in proctoring and site management preferred.
• Strong organizational, communication, and interpersonal skills.
• Ability to work independently and collaboratively.
• Proficiency in CTMS and EDC software.