Risk Surveillance Lead
Novartis
Risk Surveillance Lead
Job Description
Summary
Summary The Risk-Based Quality Management (RBQM) Risk surveillance Lead is responsible driving the adoption of RBQM practice at trial level and oversee the implementation, and continuous improvement. Risk Surveillance Lead works within a matrix environment and has overall account-ability for the surveillance of the quality risks across the assigned trials and program, enabling a comprehensive clinical quality (GCP) risk governance. The role demonstrates leadership in influencing and improving clinical trial quality through the expert understanding of clinical trial protocols, processes, regulatory requirements, and quality management principles.This role can be based in our offices in Dublin, Ireland or Barcelona, Spain. On site expectation of three days in the office.
#LI-hybrid
Locations
- Barcelona Gran Vía, Spain
- London (The Westworks), United Kingdom
Salary
Estimated Salary Rangemedium confidence
80,000 - 135,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Risk-Based Quality Management (RBQM)intermediate
- Risk surveillanceintermediate
- GCP (Good Clinical Practice)intermediate
- Quality risk governanceintermediate
- Clinical trial protocolsintermediate
- Regulatory requirementsintermediate
- Quality management principlesintermediate
- Leadershipintermediate
- Continuous improvementintermediate
Required Qualifications
- Experience in clinical trial quality management (experience)
- Expert understanding of clinical trial processes (experience)
Responsibilities
- Drive adoption of RBQM practices at trial level
- Oversee implementation and continuous improvement of RBQM
- Surveil quality risks across assigned trials and programs
- Enable comprehensive clinical quality (GCP) risk governance
- Influence and improve clinical trial quality
- Work in matrix environment with accountability for risk surveillance
- Work hybrid (3 days in office in Dublin or Barcelona)
Benefits
- general: Hybrid work (3 days in office)
Answer 10 quick questions to check your fit for Risk Surveillance Lead @ Novartis.
10 Questions
~2 Minutes
Instant Score
Risk Surveillance Lead
Novartis
Risk Surveillance Lead
Job Description
Summary
Summary The Risk-Based Quality Management (RBQM) Risk surveillance Lead is responsible driving the adoption of RBQM practice at trial level and oversee the implementation, and continuous improvement. Risk Surveillance Lead works within a matrix environment and has overall account-ability for the surveillance of the quality risks across the assigned trials and program, enabling a comprehensive clinical quality (GCP) risk governance. The role demonstrates leadership in influencing and improving clinical trial quality through the expert understanding of clinical trial protocols, processes, regulatory requirements, and quality management principles.This role can be based in our offices in Dublin, Ireland or Barcelona, Spain. On site expectation of three days in the office.
#LI-hybrid
Locations
- Barcelona Gran Vía, Spain
- London (The Westworks), United Kingdom
Salary
Estimated Salary Rangemedium confidence
80,000 - 135,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Risk-Based Quality Management (RBQM)intermediate
- Risk surveillanceintermediate
- GCP (Good Clinical Practice)intermediate
- Quality risk governanceintermediate
- Clinical trial protocolsintermediate
- Regulatory requirementsintermediate
- Quality management principlesintermediate
- Leadershipintermediate
- Continuous improvementintermediate
Required Qualifications
- Experience in clinical trial quality management (experience)
- Expert understanding of clinical trial processes (experience)
Responsibilities
- Drive adoption of RBQM practices at trial level
- Oversee implementation and continuous improvement of RBQM
- Surveil quality risks across assigned trials and programs
- Enable comprehensive clinical quality (GCP) risk governance
- Influence and improve clinical trial quality
- Work in matrix environment with accountability for risk surveillance
- Work hybrid (3 days in office in Dublin or Barcelona)
Benefits
- general: Hybrid work (3 days in office)
Answer 10 quick questions to check your fit for Risk Surveillance Lead @ Novartis.
10 Questions
~2 Minutes
Instant Score