Senior Country Clinical Quality Management Lead (Remote)

Job Description

It is critical that, for all company-sponsored clinical trials, patient safety, high quality data and compliance with company requirements and regulations are delivered and sustained. The Sr CCQM Lead supports large to medium size country/cluster clinical trial operations to achieve those objectives.  

Under the guidance of the Regional Director, Clinical Quality Management (RCQM), and in collaboration with the Clinical Research Director(s), the Sr CCQM Lead establishes and/or local clinical Quality Management System (CCQMs) aiming to achieve the organizational strategic goals and business objectives.  

The role is responsible for oversight of all CQM activities in a country/cluster of countries, or to collaboratively oversee all CQM activities in a country with multiple CRDs aligned along TA and/or functional lines. This includes line management of Country Clinical Quality Managers (CCQMs) and Associate Country Clinical Quality Managers (ACCQMs) as well as talent development in collaboration with RCQM.  

The role requires the ability to properly oversee and/or lead local quality operations to implement local/regional/global processes/procedures, to identify opportunities for process improvement, and to support continuous improvement initiatives. Advanced skills in strategic thinking, project management, ability to lead during ambiguity, analysis and risk-based decision-making and stakeholder management are required for this role.  

In addition, the Sr CCQM Lead supports audits, inspections, quality issue management as well as Quality Control and local training activities, as needed.   

Qualifications:  

• Bachelor's Degree.

• Advanced degree (e.g., Master’s Degree, PhD) preferred.  

Experience:  

• A minimum of 10 years of relevant experience in clinical research including direct field monitoring experience or management/oversight of such individuals, with a demonstrated record of accomplishments. Experience in Country Operations preferred. 

• Minimum of 2 years´ experience in a functional and/or line management position.

• Deep knowledge and understanding of Clinical Trial processes, GCP and applicable clinical research-related regulations.

• Solid track record of initiating, planning and delivery of projects and knowledge of project management practices.  

• Demonstrated experience in leading cross-functional teams.

• Experience in Clinical Quality Management including Quality Control Activities, Process Management & Improvement.  

• Demonstrated, stakeholder management and data analytics.  

• Demonstrated experience in people management  

• Ideally, experience in managing audits and inspections.

• Ideally, experience in coordinating and delivering training sessions.  

Skills:  

• Superior oral and written communication and leadership skills in an international environment.  

• Excellent project management, organizational, risk-based evaluation, and prioritization skills.  

• Superior leadership skills to effectively lead managers including talent development skills. Excellent teamwork skills, including conflict resolution expertise and discretion.  

• Ability to analyze, interpret, and solve complex …