Senior Clinical Field Specialist

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

Job summary

A leading company is seeking a Senior Clinical Field Specialist in Hemel Hempstead. The role involves overseeing clinical trials, training site staff, and ensuring compliance with regulatory standards. Candidates should have a relevant degree and experience in clinical research, especially in medical devices. Strong organizational and communication skills are essential for this opportunity.

Qualifications

• Experience in clinical research, especially in medical devices or CROs.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.

Responsibilities

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

Skills

Organizational skills

Communication skills

Clinical research knowledge

Data Management

Education

Bachelor’s degree in life sciences or healthcare

Master’s degree preferred

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, Hemel Hempstead

Client: The Mullings Group

Location: Hemel Hempstead, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

10

Posted:

28.06.2025

Expiry Date:

12.08.2025

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 the 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 take on advanced responsibilities.

Responsibilities:

• Train study staff on the correct use of the study device.
• Support site setup to ensure quality data collection.
• Maintain detailed records and documentation.
• Assist during live cases to support site staff.
• Authorize clinical sites for independent device use in agreement with CPM.
• Join clinical cases to ensure safe and effective 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 quality.
• Collaborate with investigators and CROs.

Regulatory Requirements 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 life sciences or healthcare; master's preferred.
• Experience in clinical research, especially in medical devices or CROs.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Proficiency in CTMS and EDC software.

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Created on 28/06/2025 by JR, United Kingdom