Senior Clinical Field Specialist

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

Job summary

A leading company in the medical device field is looking for a Senior Clinical Field Specialist to manage clinical trials and provide proctoring support. The role requires strong organizational and communication skills along with a background in life sciences. Candidates should have experience as a Clinical Research Associate, ensuring compliance and data integrity during study initiation and execution.

Qualifications

• Bachelor’s degree in life sciences or healthcare; master's preferred.
• Experience as Clinical Research Associate or similar in medical device or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines.

Responsibilities

• Train staff on study protocols and device usage.
• Manage clinical trial activities from initiation to close-out.
• Ensure accurate data collection and compliance with regulations.

Skills

Organizational Skills

Communication Skills

Proctoring Experience

Education

Bachelor’s degree in life sciences or healthcare

Master’s degree (preferred)

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Preston, Lancashire

Client: The Mullings Group

Location: Preston, Lancashire, 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 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:

• Proctoring and Case Support Duties:
• Train study staff on the correct use of the study device.
• Supervise/setup site workflow for consistent quality data collection.
• Maintain detailed proctoring records.
• Support site staff during live cases.
• Authorize sites for independent device use in agreement with CPM.
• Join clinical cases to support device use.

• Clinical Trial Support:
• Manage clinical trial activities from initiation to close-out.
• Train staff on study protocols, software, and regulatory requirements.
• Conduct site visits ensuring adherence and data integrity.
• Collaborate with investigators and CROs.

Regulatory Requirements Support:

• Assist in IRB submissions and audits.
• Ensure compliance with regulatory requirements.

Data Management:

• Ensure accurate data collection and resolve discrepancies.

Qualifications:

• Bachelor’s degree in life sciences or healthcare; master's preferred.
• Experience as Clinical Research Associate or similar in medical device or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency in CTMS and EDC software.