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Managing a disease area within Medical Safety, developing physician and scientist expertise in a major pharmaceutical company. Medical Degree, PhD/PharmD, Specialty Board certification, and 7+ years drug development experience required. Leading global safety programs, fostering associate career development.
Requirements
- Medical Degree or equivalent
- PhD, PharmD or equivalent graduate level health care professional degree
- Specialty Board certification
- 5 years clinical experience postdoctoral
- At least 7 years progressive experience in drug development in a major pharmaceutical company
- 5 years in safety at a medical position
- Expertise in preparing clinical safety assessments and regulatory reports
- Strong experience in leading cross-functional, multicultural teams
- Strong experience with safety issue management
- Strong experience in drug development and clinical trial methodology
- Strong leadership skills including coaching and motivating
- Post graduate degree in Pharmaceutical Medicine or Master of Public Health in Epidemiology
- Strong negotiation and conflict management skills
- Strong experience with medical writing and delivering high quality documents
- Fluent English (both spoken and written)
- Additional languages are an advantage
Tasks
- Manage the disease area within the Medical Safety organization
- Enhance the scientific and clinical experience of Medical Safety physicians and scientists
- Prepare safety objectives and evaluate performance of Medical Safety associates
- Identify and discuss high-potential associates with the leadership team
- Support associates in their career development opportunities
- Provide expert safety input to clinical development programs for assigned projects
- Participate in the Global Program Team, Global Clinical Team, and Clinical Trial Team
- Manage safety issues from the formation of the Global Program Team through Life Cycle Management
- Oversee signal detection, monitoring, evaluation, and management of safety information
- Document and track medical safety activities for assigned compounds
- Respond to inquiries from regulatory authorities and healthcare professionals on safety issues
- Lead the preparation of safety strategies for health authority responses
- Contribute to the development of departmental and functional goals and objectives
- Deputize for the Development Unit Head of Neuroscience as needed
Work Experience
- 7 years
Education
- Master's degree
Languages
- English – Native
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Managing a disease area within Medical Safety, developing physician and scientist expertise in a major pharmaceutical company. Medical Degree, PhD/PharmD, Specialty Board certification, and 7+ years drug development experience required. Leading global safety programs, fostering associate career development.
Requirements
- Medical Degree or equivalent
- PhD, PharmD or equivalent graduate level health care professional degree
- Specialty Board certification
- 5 years clinical experience postdoctoral
- At least 7 years progressive experience in drug development in a major pharmaceutical company
- 5 years in safety at a medical position
- Expertise in preparing clinical safety assessments and regulatory reports
- Strong experience in leading cross-functional, multicultural teams
- Strong experience with safety issue management
- Strong experience in drug development and clinical trial methodology
- Strong leadership skills including coaching and motivating
- Post graduate degree in Pharmaceutical Medicine or Master of Public Health in Epidemiology
- Strong negotiation and conflict management skills
- Strong experience with medical writing and delivering high quality documents
- Fluent English (both spoken and written)
- Additional languages are an advantage
Tasks
- Manage the disease area within the Medical Safety organization
- Enhance the scientific and clinical experience of Medical Safety physicians and scientists
- Prepare safety objectives and evaluate performance of Medical Safety associates
- Identify and discuss high-potential associates with the leadership team
- Support associates in their career development opportunities
- Provide expert safety input to clinical development programs for assigned projects
- Participate in the Global Program Team, Global Clinical Team, and Clinical Trial Team
- Manage safety issues from the formation of the Global Program Team through Life Cycle Management
- Oversee signal detection, monitoring, evaluation, and management of safety information
- Document and track medical safety activities for assigned compounds
- Respond to inquiries from regulatory authorities and healthcare professionals on safety issues
- Lead the preparation of safety strategies for health authority responses
- Contribute to the development of departmental and functional goals and objectives
- Deputize for the Development Unit Head of Neuroscience as needed
Work Experience
- 7 years
Education
- Master's degree
Languages
- English – Native
About the Company
Novartis
Industry
Pharmaceuticals
Description
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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