Senior Clinical Field Specialist

JR United Kingdom; Worcester; On-site; GBP 45,000 - 65,000; Full time

Job summary

A leading medical devices company is seeking a Senior Clinical Field Specialist to manage clinical trials and support staff training. This role will oversee the implementation of a novel device to improve heart attack treatments and involves significant regulatory compliance and data management responsibilities.

Qualifications

• Bachelor’s degree in a relevant field; master’s preferred.
• Experience as Clinical Research Associate or Specialist.
• Proficiency in CTMS and EDC software.

Responsibilities

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

Skills

Organizational skills

Communication skills

Knowledge of GCP

Knowledge of ISO14155

Knowledge of ICH guidelines

Education

Bachelor’s degree in a relevant field

Master’s degree (preferred)

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, Worcester

Client: The Mullings Group

Location: Worcester, 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, support clinical activities, and take on advanced proctoring responsibilities.

Responsibilities:

• Train study staff on the correct use of the study device.
• Supervise site workflow setup to ensure quality data collection.
• Maintain detailed proctoring records.
• Support site staff during live cases.
• Authorize independent use of the study device at clinical sites.
• Join clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out.
• Train and educate 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.
• Ensure compliance with regulatory requirements.

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, Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines.
• 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.