Senior Clinical Field Specialist

JR United Kingdom; Oxford; On-site; GBP 50,000 - 75,000; Full time

Job summary

A leading medical device company is seeking a Senior Clinical Field Specialist to oversee clinical trials and manage proctoring tasks for their innovative technology during PCI. The ideal candidate will have a background in life sciences, strong organizational skills, and expertise in regulatory compliance. This role involves collaboration with CROs and site management to ensure quality data collection and study integrity.

Qualifications

• Experience as Clinical Research Associate, Clinical Specialist, or similar in medical device or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Ability to work independently and in a team.

Responsibilities

• Manage clinical trial activities from initiation to close-out in collaboration with the CPM.
• Train assigned study staff on the correct use of the study device.
• Support audits and inspections at study sites.

Skills

Organizational skills

Communication skills

Education

Bachelor’s degree in life sciences

Master’s degree preferred

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, Oxford District

Client: The Mullings Group

Location: Oxford District, 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, drive clinical activity for this novel technology, and take on advanced proctoring responsibilities.

Responsibilities:

• Proctoring and Case Support Duties:
• Train assigned study staff on the correct use of the study device.
• Supervise/setup the site workflow to ensure quality data collection.
• Maintain detailed proctoring records and documentation.
• Support site staff during live cases.
• Authorize clinical sites for independent use of the study device in agreement with CPM.
• Join clinical cases to support safe device use.

• Clinical Trial Support:
• Manage clinical trial activities from initiation to close-out in collaboration with the CPM.
• Train site staff on study procedures, software, and regulatory requirements.
• Conduct site visits for qualification, initiation, monitoring, and close-out.
• Collaborate with investigators and sites to resolve issues and ensure data integrity.
• Work closely with CRO managing the clinical study.

• Regulatory Requirements Support:
• Assist in IRB submissions and documentation.
• Support audits and inspections at study sites.

• Data Management:
• Ensure accurate data collection and resolution of discrepancies.
• Collaborate with Data Management team for data quality.

Qualifications:

• Bachelor’s degree in life sciences or healthcare; master’s preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar in medical device or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Experience in proctoring and site management preferred.
• Strong organizational and communication skills.
• Ability to work independently and in a team.
• Proficiency in CTMS and EDC software solutions.