Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist in Bristol to oversee clinical trials and support innovative technology. This role involves proctoring, managing clinical activities, and ensuring compliance with regulatory standards in a dynamic setting. Ideal candidates will have a strong background in life sciences and previous proctoring experience.

Qualifications

• Experience as Clinical Research Associate or Clinical Specialist.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Ability to work independently and in teams.

Responsibilities

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

Skills

Organizational skills

Communication skills

Proctoring experience

Education

Bachelor’s in life sciences or healthcare

Master’s preferred

Tools

CTMS

EDC software

Job description

Social network you want to login/join with:

Senior Clinical Field Specialist, bristol

col-narrow-left

Client:

The Mullings Group

Location:

bristol, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

6

Posted:

26.06.2025

Expiry Date:

10.08.2025

col-wide

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 clinical activities for this innovative technology.

Responsibilities:

Proctoring and Case Support Duties:

• Train study staff on the correct use of the study device.
• Support site setup to ensure consistent quality of images and measurements.
• Maintain detailed records of proctoring activities.
• Assist during live cases to support safe device use.
• Authorize sites for independent device use in agreement with CPM.
• Join clinical cases to support device application.

Clinical Trial Support:

• Manage clinical trial activities from initiation to close-out.
• Train site staff on study procedures and software tools.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Collaborate with investigators and resolve data issues.

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 in life sciences or healthcare; master’s preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Proven proctoring and site management experience preferred.
• Strong organizational and communication skills.
• Ability to work independently and in teams.
• Proficiency with CTMS and EDC software.