Senior Clinical Field Specialist

JR United Kingdom; Guildford; On-site; GBP 40,000 - 70,000; Full time

Job summary

A leading company in the medical device field is seeking a Senior Clinical Field Specialist in Guildford. The role involves supporting clinical trials with a novel device aimed at improving heart attack treatments. Responsibilities include overseeing trial activities, training staff, and ensuring compliance with regulatory standards. Candidates should possess a relevant degree and experience in clinical research or a related field, demonstrating strong organizational and communication skills.

Qualifications

• Bachelor's degree required, master's preferred.
• Experience in medical device or CRO industry necessary.
• Knowledge of GCP, ISO14155, ICH guidelines is essential.

Responsibilities

• Manage clinical trial activities from initiation to close-out.
• Train study staff on protocols and device usage.
• Conduct site monitoring and ensure data integrity.

Skills

Organizational skills

Communication

Interpersonal skills

Attention to detail

Education

Bachelor’s degree in life sciences or healthcare

Master's degree (preferred)

Tools

CTMS software

EDC software solutions

Job description

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Senior Clinical Field Specialist, Guildford

Client: The Mullings Group

Location: Guildford, 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 both 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 help drive clinical activity for their novel technology, oversee and manage clinical trials, 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/support the setup of site workflows to ensure consistent quality of study images and measurements.
• Maintain detailed proctoring records and documentation.
• Assist during live cases by supporting site staff.
• Release clinical sites to independent use of the study device in agreement with CPM.
• Join occasional clinical cases to support safe and effective device use.

• Clinical Trial Support:
• Manage clinical trial activities from study initiation to close-out, in collaboration with the clinical project manager.
• Train and educate site staff on study protocols, use of EDC software, eISF, and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits to ensure adherence and data integrity.
• Collaborate with investigators and study staff to resolve issues and ensure timely data collection.
• Work closely with CRO managing the overall study.

• Regulatory Requirements Support:
• Assist in preparing IRB submissions and documents.
• Support audits and inspections at study sites, ensuring compliance.

• Data Management:
• Ensure accurate and timely data collection in eCRF, monitoring, and validation.
• Collaborate with Data Management team to resolve data discrepancies.

Qualifications:

• Bachelor’s degree in a relevant life science or healthcare field; 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 skills and attention to detail.
• Good communication and interpersonal skills.
• Ability to work independently and in a team in a fast-paced environment.
• Proficiency in CTMS and EDC software solutions.