Senior Clinical Field Specialist

JR United Kingdom; Doncaster; On-site; GBP 40,000 - 70,000; Full time

Job summary

A leading company in medical device innovation is looking for a Senior Clinical Field Specialist to oversee clinical activities and trials. This role involves training site staff, supporting the effective use of a novel treatment device, and managing trial processes across Europe. Candidates should possess a relevant Bachelor's or Master's degree and experience in the medical device industry, with strong organizational and communication skills.

Qualifications

• Experience as a Clinical Research Associate or similar in medical devices.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.

Responsibilities

• Train staff on the study device and procedures.
• Manage clinical trial activities from initiation to close-out.
• Support site staff during live procedures.

Skills

Organizational skills

Communication skills

Teamwork

Education

Bachelor’s degree in health science or related field

Master’s degree

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, Doncaster

Client: The Mullings Group

Location: Doncaster, United Kingdom

Job Category: Other

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EU work permit required: Yes

Job Views:

7

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 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 their innovative 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 the setup of site workflows to ensure consistent quality of images and measurements.
• Maintain detailed proctoring records and documentation.
• Support site staff during live cases.
• Coordinate with CPM to release clinical sites for independent use of the device.
• Join clinical cases to support safe and effective device use.
• Manage clinical trial activities from initiation to close-out in collaboration with the CPM.
• Train site staff on study procedures, software, and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Collaborate with investigators and study staff to resolve issues and ensure data integrity.
• Work closely with the CRO managing the overall 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 to resolve discrepancies.

Qualifications:

• Bachelor’s degree in a relevant health science or related field; Master’s preferred.
• Experience as a Clinical Research Associate, Clinical Specialist, or similar in medical devices or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory standards.
• Experience in proctoring and site management is preferred.
• Strong organizational and communication skills.
• Ability to work independently and in a team.
• Proficiency in CTMS and EDC software.

Note: If you are not a passport holder of the country for this vacancy, a work permit may be required. For more information, check our Blog.

Applicants should apply via the 'Apply now' button. Do not provide bank or payment details.

Created on 26/06/2025 by JR United Kingdom