Senior Clinical Field Specialist

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

Job summary

A leading medical technology firm is seeking a Senior Clinical Field Specialist in Milton Keynes. In this role, you will support innovative cardiac treatment methodologies by managing clinical trials, training staff, and ensuring compliance with regulatory standards. Qualified candidates should possess a degree in life sciences or healthcare, along with experience in clinical research.

Qualifications

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

Responsibilities

• Manage clinical trial activities from initiation to close-out.
• Train study staff on the correct use of the study device.
• Support site staff during live cases.

Skills

Organizational skills

Communication skills

Data Management

Education

Bachelor’s degree in a relevant life science or healthcare field

Master’s degree in a relevant field

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Milton Keynes

Client: The Mullings Group

Location: Milton Keynes

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 drive clinical activity for this innovative technology. The role involves overseeing and managing clinical trials and taking on advanced proctoring responsibilities.

Responsibilities:

• Proctoring and Case Support:
• Train study staff on the correct use of the study device.
• Supervise setup of site workflows to ensure quality data collection.
• Maintain detailed records and documentation.
• Support site staff during live cases.
• Authorize clinical sites for independent use of the device in agreement with CPM.
• Join clinical cases to support device use.

• Clinical Trial Support:
• Manage clinical trial activities from initiation to close-out.
• Train site staff on study procedures and software.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs to resolve issues.

• Regulatory Support:
• Assist in IRB submissions and audits.

• Data Management:
• Ensure accurate data collection and collaborate with Data Management team to resolve discrepancies.

Qualifications:

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