Senior Clinical Field Specialist

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

Job summary

A leading company in medical device innovation is seeking a Senior Clinical Field Specialist based in High Wycombe. This role involves overseeing clinical trials, supporting site staff, and ensuring compliance with regulatory standards. The successful candidate will have a strong background in clinical trials, regulatory knowledge, and the ability to work independently as well as within teams. Join us to contribute to groundbreaking advancements in heart attack treatment.

Qualifications

• Experience as Clinical Research Associate, Clinical Specialist, or similar.
• Strong knowledge of GCP, ISO14155, ICH guidelines.
• Preferred experience in proctoring and site management.

Responsibilities

• Train study staff on device use and ensure quality data collection.
• Manage clinical trial activities from initiation to close-out.
• Conduct site visits to ensure compliance and data integrity.

Skills

Organizational Skills

Communication Skills

Teamwork

Independence

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, High Wycombe

Client:

The Mullings Group

Location:

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

Responsibilities:

• Train study staff on the correct use of the device.
• Support site setup to ensure quality data collection.
• Maintain detailed records of proctoring activities.
• Assist during live cases to support site staff.
• Authorize clinical sites for independent device use.
• Join clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out.
• Train and educate site staff on study procedures and software.
• 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.

Qualifications:

• Bachelor’s degree in a relevant life science or healthcare field; master’s preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar in medical devices or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Ability to work independently and in teams.
• Proficiency in CTMS and EDC software.