375415BR
Nov 20, 2023
Hungary
About the Role
100,000+ That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations is Novartis’ powerhouse, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine – imagine the impact you could have as a Clinical Research Associate
.
Major responsibilities:
Your responsibilities include, but are not limited to:
• Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards.
• Ability to effectively implement and track complex projects.
• Adherence to Novartis policy and guidelines and external regulations
• Contribute to various operational aspects of assigned clinical trials /projects, under appropriate oversight responsible for certain areas of trial site selection, activation, enrolment, monitoring resource allocation, timelines and budget commitments are delivered per established trial objectives
• Involved in various operational excellence activities like process improvement or other line function initiatives.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
.
Major responsibilities:
Your responsibilities include, but are not limited to:
• Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards.
• Ability to effectively implement and track complex projects.
• Adherence to Novartis policy and guidelines and external regulations
• Contribute to various operational aspects of assigned clinical trials /projects, under appropriate oversight responsible for certain areas of trial site selection, activation, enrolment, monitoring resource allocation, timelines and budget commitments are delivered per established trial objectives
• Involved in various operational excellence activities like process improvement or other line function initiatives.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
Diversity & Inclusion / EEO
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
Minimum requirements:
What you'll bring to the role:
• Degree qualified in relevant life sciences qualification.
• 6 years’ plus experience in clinical trial monitoring in pharmaceutical and or clinical research organization.
• Team player with high learning agility and ability to adapt quickly.
• Effective communication skills.
• Excellent planning, organizing and time management skills.
• High level proficiency and ability to participate on international/ regional meetings as presenter and ability to discuss complex concepts and to negotiate effectively in English.
• B drive license
• Advanced knowledge of Ms Office, web-based and mobile apps
Why Novartis?
236 million lives were touched by Novartis medicines in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Novartis!
What you'll bring to the role:
• Degree qualified in relevant life sciences qualification.
• 6 years’ plus experience in clinical trial monitoring in pharmaceutical and or clinical research organization.
• Team player with high learning agility and ability to adapt quickly.
• Effective communication skills.
• Excellent planning, organizing and time management skills.
• High level proficiency and ability to participate on international/ regional meetings as presenter and ability to discuss complex concepts and to negotiate effectively in English.
• B drive license
• Advanced knowledge of Ms Office, web-based and mobile apps
Why Novartis?
236 million lives were touched by Novartis medicines in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Novartis!
Development
GCO GDD
Hungary
Budapest
Hungary
Research & Development
Full Time
Regular
No
