Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist to drive clinical activity for novel medical device technology. This role involves overseeing clinical trials, managing site workflows, and training staff, ensuring compliance with regulatory requirements. Ideal candidates hold a relevant degree with strong organizational and communication skills, and have experience in clinical research.

Qualifications

• Experience in clinical research or related roles required.
• Strong organizational and communication skills needed.
• Proficiency with CTMS and EDC software is important.

Responsibilities

• Train study staff on the correct use of the study device.
• Manage clinical trial activities from initiation to close-out.
• Ensure compliance with regulations and resolve data discrepancies.

Skills

Organizational skills

Communication skills

Knowledge of GCP

Knowledge of ISO14155

Knowledge of ICH guidelines

Education

Bachelor’s degree in a relevant field

Master’s degree preferred

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, Swindon, Wiltshire

Client: The Mullings Group

Location: Swindon, Wiltshire, 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 outcomes for patients. However, successful re-opening of the 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 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 activity for our client's novel technology, oversee and manage clinical trials, and take on advanced proctoring responsibilities.

Responsibilities:

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

Regulatory Requirements Support:

• Assist in IRB submissions and audits.
• Ensure compliance with regulations.

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in a relevant field; master’s preferred.
• Experience in clinical research or related roles.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency with CTMS and EDC software.