Senior Clinical Field Specialist

JR United Kingdom; Telford; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading company is seeking a Senior Clinical Field Specialist in Telford to oversee clinical trials for an innovative medical device. The role involves proctoring, training site staff, and ensuring compliance with regulatory standards. The ideal candidate will have a background in life sciences and experience in the medical device industry, with strong organizational and communication skills.

Qualifications

• Relevant experience in Clinical Research Associate or Clinical Specialist role.
• Knowledge of GCP, ISO14155, and ICH guidelines.
• Experience in proctoring and site management preferred.

Responsibilities

• Manage clinical trial activities from initiation to close-out.
• Conduct site visits to ensure data integrity.
• Support site staff during live cases.

Skills

Organizational skills

Communication skills

Interpersonal skills

Ability to work independently

Proficiency in CTMS and EDC software

Education

Bachelor’s degree in a relevant life science

Master’s degree

Job description

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Senior Clinical Field Specialist, Telford

Client: The Mullings Group

Location: Telford, 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 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/setup the site workflow for consistent quality of images and measurements.
• Maintain detailed proctoring records and documentation.
• Assist during live cases to support 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 use of the device.

• Clinical Trial Support
• Manage clinical trial activities from study initiation to close-out, collaborating with the clinical project manager.
• Train and educate site staff on study procedures, software, and regulatory requirements.
• Conduct site visits to ensure adherence and data integrity.
• Collaborate with investigators, site staff, and CROs to resolve issues and ensure data quality.

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

• Data Management
• Ensure accurate and timely data collection and resolution of discrepancies.

Qualifications:

• Bachelor’s degree in a relevant life science or healthcare field; master’s preferred.
• Experience as a 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 is preferred.
• Strong organizational, communication, and interpersonal skills.
• Ability to work independently and in a team in a fast-paced environment.
• Proficiency in CTMS and EDC software solutions.