Country Clinical Quality Manager

Gbr - London - London (moorgate Wework)mid

OtherClinical

2 views0 saves0 applied

Apply Now

Quick Summary

Key Responsibilities

Regulatory & Process Leadership: Act as the local authority on ICH-GCP and evolving UK clinical trial regulations. Partner closely with Country Operations Management to maintain robust SOPs,

Requirements Summary

Manage quality evaluations and requalifications of locally selected vendors and clinical suppliers, ensuring our high quality management system (QMS) standards are upheld.

Technical Tools

OtherClinical

Job Description

Responsibilities

~1 min read

Requirements

~1 min read

- Exceptional written and verbal communication skills with the diplomacy to navigate complex regulatory discussions.
- Strong root-cause problem solving and objective, strategic analytical capability.
- High ethical integrity, discretion, and a collaborative, solutions-oriented approach to conflict resolution.
No Travel Required

What We Offer

~1 min read

By joining our organization, you become an essential link in bringing groundbreaking therapies to patients who need them most. We offer:

Clinical Quality Management, Clinical Research, Clinical Study Design, Clinical Trial Planning, Clinical Trials Monitoring, Conflict Management, Good Clinical Practice (GCP), Operational Quality, Performance Auditing, Process Improvements, Quality Control Management, Regulatory Compliance, Risk Management