Senior Clinical Field Specialist

JR United Kingdom; Cambridge; On-site; GBP 45,000 - 70,000; Full time

Job summary

A leading company in medical innovation seeks a Senior Clinical Field Specialist to oversee and manage clinical trials across Europe. In this role, you will be responsible for training staff, ensuring compliance, and supporting clinical activities with a first-in-class medical device. Ideal candidates possess strong organizational skills and a relevant degree, aiming to make a significant impact within the medical community.

Qualifications

• Bachelor’s degree in a relevant field; master's preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.

Responsibilities

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

Skills

Organizational Skills

Communication Skills

Knowledge of GCP

Software Proficiency

Education

Bachelor’s degree in relevant field

Master’s degree (preferred)

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Cambridge

Client:

The Mullings Group

Location:

Cambridge, UK

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, the 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 clinical activities, and take on advanced proctoring responsibilities.

Responsibilities:

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

Regulatory Requirements Support:

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

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in a relevant field; master’s preferred.
• Experience as Clinical Research Associate, Clinical 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.