Senior Clinical Field Specialist

JR United Kingdom; Ipswich; On-site; GBP 40,000 - 65,000; Full time

Job summary

A leading company is seeking a Senior Clinical Field Specialist in Ipswich to manage and oversee clinical trials for a cutting-edge medical device. This role requires expertise in clinical research, regulatory compliance, and strong communication skills. The ideal candidate will work closely with study staff and contribute significantly to the success of clinical activities.

Qualifications

• Bachelor’s degree in a relevant life science or healthcare field; master's preferred.
• Experience as Clinical Research Associate, Clinical Specialist, or similar required.
• Knowledge of GCP, ISO14155, ICH guidelines.

Responsibilities

• Manage clinical trial activities from initiation to close-out.
• Train study staff on the correct use of the study device.
• Support site staff during live cases.

Skills

Organizational skills

Communication skills

Proctoring experience

Teamwork

Independence

Education

Bachelor’s degree in life science or healthcare

Master’s degree (preferred)

Tools

CTMS software

EDC software

Job description

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Senior Clinical Field Specialist, Ipswich

Client: The Mullings Group

Location: Ipswich

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 narrowed 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 and proctor clinical activities, and take on advanced responsibilities.

Responsibilities:

• Train study staff on the correct use of the study device.
• Supervise site workflow setup to ensure quality data collection.
• Maintain detailed records and documentation.
• 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 in collaboration with the CPM.
• Train and educate staff on study procedures and regulatory requirements.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Collaborate with investigators and site staff to resolve issues.
• Work closely with the CRO managing the study.

Regulatory Support:

• Assist in IRB submissions and documentation.
• Support audits and inspections, ensuring compliance.

Data Management:

• Ensure accurate data collection and validation.
• Collaborate with Data Management to resolve 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.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Proven proctoring and site management experience preferred.
• Strong organizational and communication skills.
• Ability to work independently and in a team.
• Proficiency in CTMS and EDC software.