Job ID 303797BR Position Title Global Program Regulatory Manager (80-100%*) Apply to Job
Job Description
33 major submissions. 24 major approvals. 5 new molecular entities. That was 2019. Help us continue reimagining medicine in 2020 by reimagining your career at Novartis. Our Global Regulatory Affairs (RA) group features a wide array of accomplished professionals and recent hires for an ideal blend of experience, talent, and diversity. And you could be a part of this cutting-edge team. Consider the possibilities via a career at one of the top-tier pharmaceutical companies. Our focus includes pursuing an extraordinary pipeline of promising medicines, exploring data and digital innovations, providing access to patients around the world, and helping sustain the environment for decades to come. Flexible, family friendly work arrangements ensure you have time to balance everything that’s important to you while contributing to an organization that’s dedicated to enhancing patients’ lives, including pursuing potential treatments for intriguing rare disease conditions with unmet needs. Because we are OneNovartis, OneRA, and one world at large. Read on for details on how you can take your career in an exciting direction and become part of our global community.
Join the fight against Malaria! The Tropical Medicine Regulatory Affairs team are looking for a Global Program Regulatory Manager (GPRM) to join the team in working on providing Malaria treatments to patients around the world. The GPRM in Tropical Medicines will work as part of the RA Subteam for programs through development, registration and approval/post approval.
Your responsibilities will include:
• Responsible for implementing regulatory strategy and managing operational activities for assigned projects and regions
• Represent Regulatory Affairs and lead sub-teams as required
• Health Authority interaction
• Successful implementation of global regulatory strategy for timely submissions and approvals
• Determine requirements and sets objectives for Health Authority (HA) interactions with Regulatory Affairs Project Team representative
Minimum requirements
What you’ll bring to the role:
• Science Degree
• Minimum of two years of Regulatory Affairs experience
• Fluent English
• Interest in product regulation in Africa and Asia
Why consider Novartis?
799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.
Imagine what you could do at Novartis!
*Some restrictions on flexible working options may apply and will be discussed during interview if applicable
Commitment to Diversity & Inclusion:
Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential.
Join our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here:
talentnetwork.novartis.com/network Division Global Drug Development Business Unit REG AFFAIRS GDD Location Switzerland Site Basel Company/Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No
