Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist to oversee clinical trials for a groundbreaking medical device. You'll manage proctoring responsibilities and support clinical teams, ensuring high-quality data collection and regulatory compliance. This role requires a strong educational background in life sciences and relevant clinical research experience.

Qualifications

• Bachelor’s in life sciences or healthcare, Master’s preferred.
• Experience as Clinical Research Associate or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.

Responsibilities

• Train study staff and support site setup.
• Manage clinical trial activities from initiation to close-out.
• Collaborate with investigators and resolve issues.

Skills

Organizational skills

Communication skills

Knowledge of GCP

Education

Bachelor's in life sciences or healthcare

Master's preferred

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Leeds, West Yorkshire

Client: The Mullings Group

Location: Leeds, West Yorkshire, 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 device, and take on advanced proctoring responsibilities.

Responsibilities:

• Train study staff on device use.
• Support site setup to ensure quality data collection.
• Maintain proctoring records.
• Assist during live cases.
• Authorize independent use of the device at clinical sites.
• Join clinical cases for support.
• Manage clinical trial activities from initiation to close-out.
• Train site staff on study procedures and software.
• Conduct site visits for qualification, initiation, monitoring, and close-out.
• Collaborate with investigators and resolve issues.
• Work with CROs managing the study.

Regulatory Requirements Support:

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

Data Management:

• Ensure accurate data collection.
• Resolve data discrepancies.

Qualifications:

• Bachelor’s in life sciences or healthcare, Master’s preferred.
• Experience as Clinical Research Associate 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.