Senior Clinical Field Specialist

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

Job summary

A leading company in medical technology is seeking a Senior Clinical Field Specialist to manage clinical activities for a groundbreaking device aimed at improving patient outcomes during PCI procedures. The ideal candidate will have experience in clinical trials, regulatory compliance, and a strong background in training and overseeing clinical staff.

Qualifications

• Bachelor's degree required; Master's preferred.
• Experience as Clinical Research Associate or similar role.
• Knowledge of GCP, ISO14155, and ICH guidelines.

Responsibilities

• Train staff on the use of the study device.
• Manage all clinical trial activities from start to finish.
• Ensure compliance with regulatory standards through audits.

Skills

Organizational skills

Communication skills

Proctoring

Data management

Education

Bachelor's degree in a relevant field

Master's preferred

Tools

CTMS

EDC software

Job description

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Senior Clinical Field Specialist, Peterborough

Client:

The Mullings Group

Location:

Peterborough, 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 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 drive clinical activities for this novel technology, oversee and manage clinical trials, and take on advanced proctoring responsibilities.

Responsibilities:

• Train study staff on the correct use of the study device.
• Supervise setup of site workflows to ensure quality data collection.
• Maintain detailed records and documentation.
• Support during live cases to ensure proper use of the device.
• Authorize sites for independent device use in agreement with CPM.
• Join clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out.
• Train and educate staff on study protocols, software, and regulatory requirements.
• Conduct site visits to ensure adherence and data integrity.
• Collaborate with investigators, site staff, and CROs.

Regulatory Requirements Support:

• Assist in 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 Clinical Research Associate, Clinical 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.