Senior Global Program Safety Lead

Primary Location:  Basel, Switzerland

Alternate Location(s): Barcelona, Spain  

Working model:  Both locations have a hybrid working model (12 days per month in the office)

Closing date for applications: 18 October 2024

About this role:

Our Senior Global Program Safety Lead excels as a scientific safety leader within the Oncology Medical Safety organization.

Join us and you will make a significant impact on patients' lives and contribute to Novartis' overall success through robust safety evaluation expertise and medical innovation.

Key Responsibilities:  

• Safety Input and Team Participation: Provide expert safety input to the clinical development program for assigned projects/products and actively participate in the Global Program Team (GPT), Global Clinical Team (GCT), and Clinical Trial Team (CTT). Responsible for managing safety issues from the formation of the GPT through Life Cycle Management.
• Signal Detection and Safety Management: Oversee overall signal detection, monitoring, evaluation, interpretation, and appropriate management of safety information, based on data from all relevant line functions, post-marketing data, and other sources.
• Documentation and Record Keeping: Ensure proper documentation, tracking, and record-keeping of medical safety activities for assigned compounds.
• Regulatory and Professional Inquiries: Respond to inquiries from regulatory authorities or healthcare professionals regarding safety issues.
• Safety Strategy Preparation: Lead the preparation of the safety strategy for health authority responses and collaborate with other project team members.
• Departmental and Functional Goals: Contribute to and often lead the development of departmental and functional/business unit goals and objectives.
• Marketing Samples Distribution: Manage the distribution of marketing samples, where applicable.

Key performance indicators:

• Timeliness and quality of safety analyses, interpretations, and presentation
• Compliance with internal and external regulations & procedures
• Compliance, consistency and quality of safety deliverables

Role Requirements:

• Medical Degree is required
• 10+ years of experience in Big Pharma
• 3 to 5 years Oncology experience.

Skills:

• Clinical Research.
• Clinical Trials.
• Functional Teams.
• Leadership.
• Medical Strategy.
• Process Safety Management.
• Regulatory Compliance.
• Risk Management.
• Safety Science.

Languages :

• Fluent English (both spoken and written) is mandatory. 
• Additional languages are an advantage.

Why Novartis:  Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

Commitment to Diversity and Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network