Senior Clinical Field Specialist

JR United Kingdom; Slough; On-site; GBP 35,000 - 60,000; Full time

Job summary

A leading medical device company is seeking a Senior Clinical Field Specialist to oversee and manage clinical trials for innovative technology. The role involves training staff, ensuring compliance, and maintaining quality data collection during trials.

Qualifications

• Experience as Clinical Research Associate, Specialist, or similar.
• 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.
• Manage clinical trial activities from initiation to close-out.
• Conduct site visits to ensure compliance and data integrity.

Skills

Organizational skills

Communication skills

Education

Bachelor’s degree in life sciences or healthcare

Master’s degree

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, slough

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Client:

The Mullings Group

Location:

slough, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025

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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 both diagnose microvascular obstruction (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 activities for this novel technology, oversee and manage clinical trials, and take on advanced proctoring responsibilities.

Responsibilities:

Proctoring and Case Support Duties:

• Train study staff on the correct use of the study device.
• Supervise/setup site workflow to ensure quality data collection.
• Maintain detailed proctoring records.
• Support site staff during live cases.
• Authorize sites for independent device use.
• 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.

Regulatory Support:

• Assist with IRB submissions and audits.

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, Specialist, 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.