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Global Program Safety Lead(m/w/x)
Leading medical oversight for new drug development within clinical trial programs. Medical Degree, 5 years drug development, and 2 years safety experience required. Extensive collaboration across global clinical and program teams.
Requirements
- Medical Degree or equivalent
- 3 years clinical experience postdoctoral
- Minimum 5 years experience in drug development in a major pharmaceutical company
- 2 years in safety at an operational or medical position
- Experience in clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications
- Expertise in preparing clinical safety assessments and regulatory reports/submissions
- Experience with safety issue management
- Experience in leading cross-functional, multicultural teams
- Fluent English (both spoken and written)
- Additional languages are an advantage
Tasks
- Provide expert safety input for clinical development programs
- Participate in the Global Program Team, Global Clinical Team, and Clinical Trial Team
- Lead the Safety Management Team
- Manage safety issues throughout the project lifecycle
- Own the safety strategy for projects and products
- Produce medical safety deliverables
- Develop and maintain safety information in the Core Data Sheet
- Address safety issues across all project and product indications
- Oversee signal detection and monitoring of safety information
- Evaluate and interpret safety data from relevant sources
- Prepare safety strategies for health authority responses
- Collaborate with project team members on safety inquiries
- Respond to regulatory authorities and healthcare professionals regarding safety issues
- Contribute to departmental and functional goals and objectives
- Engage in developing competencies within the Medical Safety Function
Work Experience
- 5 years
Education
- Master's degree
Languages
- English – Business Fluent
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Global Program Safety Lead(m/w/x)
Leading medical oversight for new drug development within clinical trial programs. Medical Degree, 5 years drug development, and 2 years safety experience required. Extensive collaboration across global clinical and program teams.
Requirements
- Medical Degree or equivalent
- 3 years clinical experience postdoctoral
- Minimum 5 years experience in drug development in a major pharmaceutical company
- 2 years in safety at an operational or medical position
- Experience in clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications
- Expertise in preparing clinical safety assessments and regulatory reports/submissions
- Experience with safety issue management
- Experience in leading cross-functional, multicultural teams
- Fluent English (both spoken and written)
- Additional languages are an advantage
Tasks
- Provide expert safety input for clinical development programs
- Participate in the Global Program Team, Global Clinical Team, and Clinical Trial Team
- Lead the Safety Management Team
- Manage safety issues throughout the project lifecycle
- Own the safety strategy for projects and products
- Produce medical safety deliverables
- Develop and maintain safety information in the Core Data Sheet
- Address safety issues across all project and product indications
- Oversee signal detection and monitoring of safety information
- Evaluate and interpret safety data from relevant sources
- Prepare safety strategies for health authority responses
- Collaborate with project team members on safety inquiries
- Respond to regulatory authorities and healthcare professionals regarding safety issues
- Contribute to departmental and functional goals and objectives
- Engage in developing competencies within the Medical Safety Function
Work Experience
- 5 years
Education
- Master's degree
Languages
- English – Business Fluent
About the Company
Novartis
Industry
Healthcare
Description
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Not a perfect match?
- Novartis
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