Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist in Sheffield to oversee clinical trials for a groundbreaking medical device. The role involves proctoring, managing site activities, and ensuring compliance with regulations. Candidates should have a strong background in life sciences and experience in clinical research, alongside excellent organizational and communication skills.

Qualifications

• Bachelor’s degree in life sciences or healthcare required, Master’s preferred.
• Experience as Clinical Research Associate or Specialist.
• Knowledge of GCP, ISO14155, ICH guidelines.

Responsibilities

• Train staff on the use of the study device.
• Manage clinical activities from initiation to close-out.
• Ensure accurate data collection and resolve discrepancies.

Skills

Organizational skills

Communication

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, Sheffield, South Yorkshire

Client: The Mullings Group

Location: Sheffield, South Yorkshire, 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 clinical trials, support proctoring activities, and manage the deployment of this innovative technology.

Responsibilities:

• Proctoring and Case Support:
• Train study staff on the use of the study device.
• Supervise site setup to ensure quality data collection.
• Maintain proctoring records.
• Support site staff during live cases.
• Authorize independent use of the device at sites.
• Join clinical cases for support.

• Clinical Trial Support:
• Manage clinical activities from initiation to close-out.
• Train staff on study procedures and software.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and CROs.

• Regulatory Support:
• Assist with IRB submissions and audits.

• Data Management:
• Ensure accurate data collection and resolve discrepancies.

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.
• Proven proctoring and site management experience preferred.
• Strong organizational and communication skills.
• Proficiency with CTMS and EDC software.