Senior Clinical Field Specialist

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

Job summary

A leading medical device company is seeking a Senior Clinical Field Specialist in Watford to oversee clinical trials for cutting-edge technology. The role involves training staff, managing trial activities, and ensuring compliance with regulations. The ideal candidate will have a degree in a relevant healthcare field and experience in clinical research.

Qualifications

• Experience as a Clinical Research Associate or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.
• 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.
• Supervise site workflows and assist during live cases.

Skills

Strong organizational skills

Communication skills

Ability to work independently

Teamwork

Proficiency in CTMS

Proficiency in EDC software

Education

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

Master’s degree (preferred)

Job description

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Senior Clinical Field Specialist, Watford, Hertfordshire

Client: The Mullings Group

Location: Watford, Hertfordshire, United Kingdom

Job Category: Other

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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 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 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 workflows to ensure consistent quality of images and measurements.
• Maintain detailed proctoring records and documentation.
• Assist during live cases to support site staff.
• 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 in collaboration with the CPM.
• Train site staff on study procedures, EDC software, eISF, and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Collaborate with investigators and site staff to resolve issues and ensure data integrity.
• Work closely with the CRO managing the study.

Regulatory Requirements Support:

• Assist in preparing IRB submissions and documents.
• Support audits and inspections at study sites for compliance.

Data Management:

• Ensure accurate and timely data collection and validation.
• 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 a Clinical Research Associate, Clinical Specialist, or similar in medical device or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Ability to work independently and in a team.
• Proficiency in CTMS and EDC software solutions.