Senior Clinical Field Specialist

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

Job summary

A leading company in the medical device industry is seeking a Senior Clinical Research Specialist in Gloucester to oversee clinical trials and support innovative technology deployment across Europe. This role involves training, managing clinical activities, and ensuring compliance with regulatory standards in a dynamic environment.

Qualifications

• Experience in clinical research, especially in medical devices or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Proven proctoring and site management experience preferred.

Responsibilities

• Train study staff on the device use and supervise site workflows.
• Manage clinical trial activities from initiation to close-out, ensuring compliance and data integrity.
• Assist with IRB submissions, audits, and inspections.

Skills

Organizational Skills

Communication Skills

Software Skills

Education

Bachelor’s degree in a relevant field

Master’s degree preferred

Job description

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Senior Clinical Field Specialist, Gloucester

Client: The Mullings Group

Location: Gloucester, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 6

Posted: 26.06.2025

Expiry Date: 10.08.2025

Job Description:

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. We are hiring a Senior Clinical Research Specialist to oversee clinical trials, manage activities, and support the deployment of this innovative technology across Europe.

Responsibilities:

• Train study staff on the device use and supervise site workflows.
• Maintain detailed records and support live cases.
• Manage clinical trial activities from initiation to close-out, ensuring compliance and data integrity.
• Collaborate with investigators, site staff, and CROs.

Regulatory Support:

• Assist with IRB submissions, audits, and inspections.
• Ensure accurate data collection and collaborate with Data Management.

Qualifications:

• Bachelor’s degree in a relevant field; Master’s preferred.
• Experience in clinical research, especially in medical devices or CRO industry.
• Knowledge of GCP, ISO14155, ICH guidelines.
• Proven proctoring and site management experience preferred.
• Strong organizational, communication, and software skills.