Hybrid Clinical Study Manager, Medical Devices (EU/US Travel)

Talentmark Limited; England; Hybrid; GBP 70,000 - 110,000; Full time

Job summary

Talentmark Limited is seeking a Clinical Study Manager for a hybrid role in the UK. The position oversees international clinical studies, ensuring delivery on time, within budget, and in line with GCP, ISO 14155 and SOPs. Occasional travel to Europe and the US supports sites and trials.

The role requires extensive trial management experience, CE mark trial setup/closeout, and strong cross-functional leadership. entitlement to work in the UK is essential.

Qualifications

• Bachelor’s degree in a scientific or health-related field or equivalent.
• Extensive experience in clinical trial management for implantable neuromodulation devices.
• Experience with EU CE mark trials and strong knowledge of GCP and ISO14155.

Responsibilities

• Lead international clinical study operations, ensuring on-time, on-budget delivery.
• Manage CROs, vendors and third-party suppliers to ensure high-quality results.
• Monitor site performance, patient recruitment and operational progress.
• Ensure compliance with study protocols, GCP, ISO 14155 and SOPs.
• Collaborate cross-functionally to support product improvements and investigations.
• Build and maintain relationships with investigators and clinical sites.
• Provide operational support for clinical sites and visits.
• Support audit readiness, inspections, data integrity and queries.
• Travel regularly across Europe with occasional trips to the US.

Skills

Vendor oversight

Cross-functional leadership

Communication

Team player

Agile working

Education

Bachelor’s degree in scientific/health field

Job description

Talentmark Limited is seeking a Clinical Study Manager for a hybrid role in the UK. The position oversees international clinical studies, ensuring delivery on time, within budget, and in line with GCP, ISO 14155 and SOPs. Occasional travel to Europe and the US supports sites and trials.

The role requires extensive trial management experience, CE mark trial setup/closeout, and strong cross-functional leadership. entitlement to work in the UK is essential.