Clinical FSP Quality Manager
52865
Posted: 31/07/2026
- Competitive
- finland, United Kingdom
- Part Time
Needed - Clinical FSP Quality Manager
Remote Full time
The purpose of this role is to collaborate with global Quality Management groups, functional teams, and other stakeholders in a joint pursuit to carry out, and adopt the global quality plan according to the specific requirements defined by the scope of the assignment
About the role
• Conduct country and site-level compliance oversight using a risk-based approach.
• Identify compliance risks and conduct site assessments,
• Conduct inspections and audits
• Drive inspections and compliance at the country level.
• implement the global Quality Management Plan within the framework of the assignment, this will include Planning and executing the Quality Management activities.
• collaborate closely with the relevant business and other stakeholders, support maintaining focus on quality in project delivery.
Qualifications
• 9+ years total experience.
• Clinical Operations background, Oncology experience desirable.
• Knowledge of National and International Regulations and Drug Development processes.
• Good organizational and communication skills
• Ability to lead a clinical team.
• Fluent in English.
Remote Full time
The purpose of this role is to collaborate with global Quality Management groups, functional teams, and other stakeholders in a joint pursuit to carry out, and adopt the global quality plan according to the specific requirements defined by the scope of the assignment
About the role
• Conduct country and site-level compliance oversight using a risk-based approach.
• Identify compliance risks and conduct site assessments,
• Conduct inspections and audits
• Drive inspections and compliance at the country level.
• implement the global Quality Management Plan within the framework of the assignment, this will include Planning and executing the Quality Management activities.
• collaborate closely with the relevant business and other stakeholders, support maintaining focus on quality in project delivery.
Qualifications
• 9+ years total experience.
• Clinical Operations background, Oncology experience desirable.
• Knowledge of National and International Regulations and Drug Development processes.
• Good organizational and communication skills
• Ability to lead a clinical team.
• Fluent in English.
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