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 drivers license.
Learn more about our EEO & Accommodations request here.
Our FSPx department is looking for a Quality Control Manager you will beresponsible for (but not only):Annual country specific QC plan monitoring and coordinating the implementation and execution of QC planResponsibility for the management of the Client Corrective and Preventive actions (CAPA) of GC...
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 drivers license.
Learn more about our EEO & Accommodations request here.
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