Country Clinical Quality Manager, Remote

Scorpion Therapeutics; United States; Remote; USD 120,000 - 190,000; Full time

Job summary

Scorpion Therapeutics seeks a Country Clinical Quality Manager (CCQM) to oversee clinical quality activities across trials, ensuring patient safety, data integrity, and regulatory compliance. You will implement processes, support audits, and coordinate quality control with global teams.

The role requires a Bachelor's degree in a healthcare field and 6+ years in clinical research, with emphasis on monitoring, operations, or quality management. 10% travel and remote work setup are expected.

Qualifications

• Bachelor's degree in healthcare or related field.
• 6+ years in clinical research, with experience in monitoring, clinical operations, or quality management.
• Deep understanding of GCP and regulatory requirements.
• Experience in audits/inspections and quality control activities.
• Strong abilities in process improvement and training.

Responsibilities

• Oversee clinical quality activities in a specified country/region to ensure patient safety, data integrity, and regulatory compliance across clinical trials.
• Implement local/global processes, support audits and inspections, and manage quality control activities.
• Lead local training and coordinate issues related to compliance, privacy, and clinical supplies.
• Collaborate with local and global teams to address audit findings and quality trends.
• Support continuous process improvements and QC investigations.

Skills

GCP knowledge

Audit management

Team leadership

Quality management

Process improvement

Education

Bachelor's degree in healthcare or related field

Job description

Country Clinical Quality Manager (CCQM)

Role: Country Clinical Quality Manager (CCQM) overseeing clinical quality activities in a specified country/region to ensure patient safety, data integrity, and regulatory compliance across clinical trials.

Responsibilities include implementing local/global processes, supporting audits and inspections, managing quality control activities, leading local training, and coordinating issues related to compliance, privacy, and clinical supplies.

The CCQM manages quality-related investigations, supports continuous process improvements, and collaborates with local and global teams to address audit findings and quality trends.

Qualifications: Bachelor's in a healthcare or related field; 6+ years in clinical research, with experience in monitoring, clinical operations, or quality management.

Deep understanding of GCP, clinical trial processes, and regulatory requirements is essential.

Preferred skills include expertise in process improvement, audit management, and team leadership.

Experience in clinical quality management, including QC activities, process optimization, and inspection handling, is highly valued.

High-value specifics: focus on clinical quality in international trials, with responsibilities spanning GCP compliance, audits, inspections, and training; 10% travel; remote work setup; no direct reports; US-based scope; working with regulatory and quality standards in a clinical research environment.