Clinical Quality Manager

A company is looking for a Clinical Program Quality Manager.

Key Responsibilities

Support GCP compliance activities for oncology clinical trials through audit and compliance strategies

Conduct audits of investigator sites and internal systems to ensure adherence to GCP and regulatory requirements

Manage quality investigations and provide support during regulatory inspections

Required Qualifications

Bachelor's degree in Pharmacy, Regulatory Affairs, Clinical or related field

5 years of related experience in clinical quality management

Knowledge of GCP and GVP regulations and ICH Guidelines

Experience in identifying and investigating quality issues

Ability to manage and track team projects and timelines