Senior Clinical Field Specialist

JR United Kingdom; Stockport; On-site; GBP 50,000 - 65,000; Full time

Job summary

A leading medical device company is seeking a Senior Clinical Field Specialist in Stockport. The successful candidate will oversee clinical trials, train study staff, and support audits, ensuring high-quality data collection and compliance with regulatory standards. Ideal candidates have a relevant degree and experience in clinical research, with proficiency in CTMS and EDC software.

Qualifications

• Bachelor’s degree; experience as Clinical Research Associate or similar required.
• Experience in proctoring and site management preferred.

Responsibilities

• Train staff on study device and protocols.
• Oversee and manage clinical trials from start to finish.
• Maintain proctoring records and assist during live cases.

Skills

Organizational skills

Communication skills

Knowledge of GCP

Knowledge of ISO14155

Knowledge of ICH guidelines

Proficiency in CTMS and EDC software

Education

Bachelor’s degree in a relevant field

Master’s preferred

Job description

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Senior Clinical Field Specialist, Stockport

Client:

The Mullings Group

Location:

Stockport, 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 proctoring activities, and take on advanced responsibilities.

Responsibilities:

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

Regulatory Support:

• Assist with IRB submissions.
• Support audits and inspections.

Data Management:

• Ensure accurate data collection and collaborate with Data Management team.

Qualifications:

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