Senior Clinical Field Specialist

JR United Kingdom; Wolverhampton; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading company in medical innovation is seeking a Senior Clinical Field Specialist to manage clinical trials for a pioneering medical device. The successful candidate will oversee proctoring activities and ensure compliance with regulatory standards, making a significant impact on cardiac treatment advancements. This role requires a strong educational background in life sciences and extensive experience in clinical research management.

Qualifications

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

Responsibilities

• Train study staff on the correct use of the device.
• Manage clinical trial activities from initiation to close-out.
• Assist with IRB submissions and audits.

Skills

Strong organizational skills

Communication skills

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, Wolverhampton

Client: The Mullings Group

Location: Wolverhampton

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 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, support proctoring activities, and drive the clinical activities for this innovative technology.

Responsibilities:

Proctoring and Case Support Duties

• Train study staff on the correct use of the device.
• Supervise site setup to ensure quality data collection.
• Maintain detailed records of proctoring activities.
• Support site staff during live cases.
• Authorize independent use of the device at sites in coordination 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 procedures, software, and regulatory requirements.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs.

Regulatory Requirements Support

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

Data Management

• Ensure accurate data collection and resolve discrepancies.
• Work with Data Management team.

Qualifications:

• Bachelor’s degree in life sciences or healthcare; Master’s preferred.
• Experience as 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 in CTMS and EDC software.

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

Applications should be made via the 'Apply now' button. Do not provide bank or payment details.

Created on 26/06/2025 by JR United Kingdom