Senior Clinical Field Specialist

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

Job summary

A leading company in the medical device industry seeks a Senior Clinical Field Specialist to oversee clinical trials and manage on-site workflows in Woking. This role involves training staff, ensuring compliance with regulatory standards, and collaborating with investigators. Candidates should have a background in clinical research with strong organizational and communication skills.

Qualifications

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

Responsibilities

• Train study staff on device use.
• Supervise site workflows for data collection.
• Manage clinical trial activities from initiation to close-out.

Skills

Organizational skills

Communication skills

Education

Bachelor’s degree in a relevant field

Master’s preferred

Tools

CTMS software

EDC software

Job description

Social network you want to login/join with:

Senior Clinical Field Specialist, Woking

Client: The Mullings Group

Location: Woking, 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 and take on advanced proctoring responsibilities.

Responsibilities:

• Train study staff on the correct use of the study device.
• Supervise/setup site workflows for consistent data collection.
• Maintain detailed records and documentation.
• Support site staff during live cases.
• Authorize sites for independent device use.
• Join clinical cases to support device use.
• Manage clinical trial activities from initiation to close-out.
• Train site staff on study protocols, software, and regulatory requirements.
• Conduct site visits to ensure compliance and data integrity.
• Collaborate with investigators and the CRO.

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 degree in a relevant field; Master’s preferred.
• Experience as Clinical Research Associate, Specialist, or similar.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory standards.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency in CTMS and EDC software.