Senior Clinical Field Specialist

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

Job summary

A leading company in medical device development is seeking a Senior Clinical Field Specialist to oversee clinical trials across Europe. This role involves training staff, managing trial activities, and ensuring compliance with regulatory standards. The successful candidate will work with a cutting-edge medical device to improve patient outcomes in real-time diagnostics.

Qualifications

• Bachelor's degree in a relevant field; master's preferred.
• Experience as a Clinical Research Associate, Specialist, or similar required.
• Strong organizational and communication skills essential.

Responsibilities

• Train study staff on the use of the study device.
• Manage clinical trial activities from initiation to close-out.
• Ensure compliance with regulatory standards.

Skills

Organizational skills

Communication skills

Knowledge of GCP

Proctoring

Site management

Education

Bachelor's degree

Master's degree (preferred)

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Chester

Client: The Mullings Group

Location: Chester, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 6

Posted: 26.06.2025

Expiry Date: 10.08.2025

Job Description:

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 oversee and manage clinical trials and take on advanced proctoring responsibilities.

Responsibilities:

• Train study staff on the use of the study device.
• Support site setup to ensure quality data collection.
• Maintain detailed records of proctoring activities.
• Support live cases and assist site staff during procedures.
• Authorize sites for independent device use after approval.
• Join clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out.
• Train site staff on study protocols, software, and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Collaborate with investigators and CROs to ensure data quality.

Regulatory Support:

• Assist with IRB submissions and audits.
• Ensure compliance with regulatory standards.

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in a relevant field; master’s preferred.
• Experience as a Clinical Research Associate, Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency with CTMS and EDC software.