Senior Clinical Field Specialist

JR United Kingdom; Bolton; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading medical device company is seeking a Senior Clinical Field Specialist to drive clinical activities in Bolton. This role involves managing clinical trials for an innovative device, providing proctoring support, and ensuring compliance with regulatory requirements. Candidates should have relevant life science backgrounds and experience in clinical research or medical devices. Strong organizational and communication skills are essential for success in this dynamic setting.

Qualifications

• Experience as Clinical Research Associate or Clinical Specialist in medical device or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines, and regulatory requirements.
• Proven experience in proctoring and site management preferred.

Responsibilities

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

Skills

Organizational Skills

Attention to Detail

Communication Skills

Interpersonal Skills

Education

Bachelor’s degree in a relevant life science or healthcare field

Master’s degree (preferred)

Tools

CTMS

EDC software solutions

Job description

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Senior Clinical Field Specialist, Bolton, Greater Manchester

Client: The Mullings Group

Location: Bolton, Greater Manchester, United Kingdom

Job Category: Other

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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 outcomes for patients. 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 both diagnose microvascular obstruction (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 this innovative technology, overseeing and managing clinical trials, and taking 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 use of the device.

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

Regulatory Requirements Support:

• Assist in preparing IRB submissions and documents as needed.
• Support internal and external audits and inspections to ensure 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 degree preferred.
• Relevant experience as Clinical Research Associate, Clinical Specialist, or similar in the medical device or CRO industry.
• Good knowledge of GCP, ISO14155, ICH guidelines, and other regulatory requirements.
• Proven 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.