Our FSPx department is looking for a Quality Control Manager, you will be
responsible for (but not only):

• Annual country specific QC plan, monitoring, and coordinating the implementation, and execution of QC plan

• Responsibility for the management of the Client Corrective and Preventive actions (CAPA) of GCP audits and inspections

• Responsibility to manage and/or co-lead key Client

This role requires the ability to follow current processes and procedures of the Client but also the ability to improve processes and procedures. This position has a significant impact on the ability to conduct clinical trials in accordance with external and internal regulations and guidelines of the Client.

Experience:

• Minimum of 6-8 years of clinical research monitoring experience

• Demonstrated experience leading cross-functional teams of business professional.

• Excellent site monitoring skills.

• Excellent study site management skills.

• Excellent verbal and written communication skills in French and English.

Work Environment:

• Available for travel up to 40% of the time including overnight stays as necessary consistent with project needs and office location (this will vary based on country and project needs).

• Ability to drive and have a valid driver’s license.

Learn more about our EEO & Accommodations request here.