Senior Clinical Field Specialist

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

Job summary

A leading company in the medical device sector seeks a Senior Clinical Field Specialist in Brighton. This role involves overseeing clinical trials, training staff, managing study sites, and ensuring compliance with regulatory standards. Applicants should possess a background in life sciences and experience in clinical research.

Qualifications

• Bachelor’s degree in life sciences or healthcare; Master’s preferred.
• Experience as Clinical Research Associate or similar.
• Strong organizational and communication skills required.

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 quality.

Skills

Organizational skills

Communication skills

Education

Bachelor’s degree in life sciences or healthcare

Master’s degree (preferred)

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Brighton

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Client:

The Mullings Group

Location:

Brighton, 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 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:

Proctoring and Case Support Duties

• Train study staff on the correct use of the study device.
• Supervise site setup to ensure quality data collection.
• Maintain detailed records and documentation.
• Support site staff during live cases.
• Authorize independent use of the device at clinical sites.
• Join clinical cases to support device use.

Clinical Trial Support

• Manage clinical trial activities from initiation to close-out.
• Train staff on study procedures and software.
• Conduct site visits to ensure compliance and data quality.
• Collaborate with investigators and CROs.

Regulatory Requirements Support

• Assist with IRB submissions and audits.
• Support data management and resolve discrepancies.

Qualifications:

• Bachelor’s degree 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.