Senior Clinical Field Specialist

JR United Kingdom; Stoke-on-Trent; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading medical technology company is seeking a Senior Clinical Field Specialist in Stoke-on-Trent to support their innovative clinical trials. This role involves extensive proctoring, regulatory compliance, and managing clinical activities to ensure quality and integrity of data collection. With a focus on advancing heart attack treatment, candidates with strong clinical backgrounds and exceptional organizational skills are encouraged to apply.

Qualifications

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

Responsibilities

• Oversee clinical trials and manage activities from start to finish.
• Train study staff and ensure compliance with standards.
• Collaborate with investigators and CROs to address challenges.

Skills

Organizational skills

Communication skills

Proctoring

Site management

Education

Bachelor’s degree in a relevant field

Master’s preferred

Tools

CTMS

EDC software

Job description

Social network you want to login/join with:

Senior Clinical Field Specialist, Stoke-on-Trent

col-narrow-left

Client:

The Mullings Group

Location:

Stoke-on-Trent, 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 help drive clinical activity for this innovative technology. The role involves overseeing and managing clinical trials and taking on advanced proctoring responsibilities.

Responsibilities:

Proctoring and Case Support Duties:

• Train study staff on the correct use of the study device.
• Supervise/setup site workflows to ensure quality data collection.
• Maintain detailed records and documentation.
• Support site staff during live cases.
• 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 in collaboration with the CPM.
• Train staff on study procedures, software, and regulatory requirements.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs to resolve issues.

Regulatory Requirements Support:

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

Data Management:

• Ensure accurate data collection and collaborate with Data Management to 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, and regulatory standards.
• Proven proctoring and site management experience preferred.
• Strong organizational and communication skills.
• Ability to work independently and in teams.
• Proficiency in CTMS and EDC software.