Senior Clinical Field Specialist

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

Job summary

A leading company in healthcare technology seeks a Senior Clinical Field Specialist in Nottingham to oversee clinical trial activities for an innovative medical device. Responsibilities include proctoring, training site staff, and ensuring adherence to regulatory requirements. Applicants should have a relevant degree and experience within the medical device or CRO industry.

Qualifications

• Relevant experience as Clinical Research Associate or similar in the medical device industry.
• Good knowledge of GCP, ISO14155, ICH guidelines.
• Ability to work independently and collaboratively.

Responsibilities

• Train study staff on device use and supervise site workflow.
• Manage clinical trial activities from initiation to close-out.
• Collaborate with study site staff to ensure data integrity and compliance.

Skills

Organizational skills

Attention to detail

Communication

Interpersonal skills

Education

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

Master’s degree preferred

Tools

CTMS software

EDC software solutions

Job description

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Senior Clinical Field Specialist, nottingham

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Client:

The Mullings Group

Location:

nottingham, 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 the 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 who will help drive greenfield clinical activity for our clients novel technology, overseeing and managing clinica ltrials, and taking on advanced proctroing responsibiltites.

Responsibilities:

Proctoring and Case Support Duties

• Train assigned study staff on the correct use of the study device.
• Supervise/support the setup of the required site workflow to ensure study images and measurements are collected and of consistent quality.
• Maintain detailed proctoring records and documentation.
• Assist during live cases by supporting site staff
• In agreement with CPM, release clinical sites to independent use of the study device.
• Join occasional clinical cases to support safe and effective use of the study device.
• Clinical Trial Support.
• Manage clinical trial activities in alignment with the clinical project manager (CPM), from study initiation to close-out.
• Train and educate site staff on study CIP, the correct use of the study EDC software, the electronic Investigator Site File (eISF), and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits to ensure CIP adherence and data integrity.
• Collaborate with investigators and study site staff to resolve issues and ensure timely and accurate data collection.
• Work in close collaboration with CRO who manages the overall clinical study.

Regulatory Requirements Support

• Assist in the preparation IRB submissions and documents, as needed.
• Assist in internal and external audits and inspections at study sites, ensuring compliance with regulatory requirements.
• Data Management.
• Ensure accurate and timely data collection in eCRF, monitoring, and validation according to the CIP and associated documents.
• Collaborate with Data Management team to resolve data discrepancies with sites.

Qualifications:

• Bachelor’s degree in a relevant life science or healthcare field, master’s degree preferred.
• Relevant experience as Clinical Research Associate, Clinical Specialist or similar in the medical device or CRO industry.
• Good knowledge of GCP, ISO14155, ICH guidelines, and other relevant regulatory requirements.
• Proven experience in proctoring and site management preferred.
• Strong organizational skills and attention to detail.
• Good communication and interpersonal skills.
• Ability to work independently and collaboratively in a fast-paced environment.
• Proficiency in using CTMS and EDC software solutions.