Senior Clinical Field Specialist

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

Job summary

A leading company in medical device technology seeks a Senior Clinical Field Specialist in Birmingham to oversee clinical trials and manage proctoring duties. Ideal candidates should possess a solid background in clinical research and be adept in regulatory requirements, ensuring compliance and data integrity throughout the trials. This role offers the opportunity to work collaboratively in a fast-paced environment while driving innovative solutions in the medical field.

Qualifications

• Relevant experience as Clinical Research Associate, Clinical Specialist, or similar.
• Good knowledge of GCP, ISO14155, ICH guidelines.
• Proven experience in proctoring and site management preferred.

Responsibilities

• Supervise and support the setup of site workflows and training.
• Manage clinical trial activities from study initiation to close-out.
• Ensure accurate and timely data collection and resolve discrepancies.

Skills

Organizational skills

Attention to detail

Communication skills

Interpersonal skills

Education

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

Master’s degree (preferred)

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Birmingham

Client:

The Mullings Group

Location:

Birmingham, United Kingdom

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, treatment of heart attacks by minimally invasive percutaneous coronary intervention (PCI) has significantly improved patient outcomes. 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 their innovative technology, overseeing and managing clinical trials, and taking on advanced proctoring responsibilities.

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 managing the overall clinical study.

Regulatory Requirements Support:

• Assist in the preparation of 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.