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Clinical Project/Trial Physician(m/w/x)
Description
In this role, you will provide medical leadership and oversight for clinical projects, ensuring high-quality scientific input and guiding the Clinical Trial Team. Your day-to-day responsibilities will involve engaging with external experts, conducting safety reviews, and contributing to strategic decisions.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical degree (MD)
- •At least 5 years of experience in Clinical Development within the pharmaceutical or biotech industry
- •Clinical research or clinical practice experience in CNS and in at least one therapeutic area: Cardiovascular, Immunology, or Rheumatology
- •Strong knowledge of drug development and clinical trial process
- •Direct experience interacting with Health Authorities and understanding of regulatory requirements and ICH guidelines
- •Excellent written and spoken English skills
- •Strong organizational abilities
- •Proven success in complex matrix organizations and engaging with stakeholders
- •Hands-on, results-driven mindset with urgency and accountability
- •Proactive, solution-oriented approach
- •Analytical, data-driven thinker with attention to detail
- •Shares expertise openly and contributes to collaborative learning
- •Ability to think globally and understand broader strategic context
Education
Work Experience
5 years
Tasks
- •Provide medical leadership for assigned projects
- •Lead and oversee medical components of clinical projects
- •Ensure high-quality medical input into clinical documents
- •Contribute evidence-based insights to global clinical strategy
- •Offer medical and scientific guidance to the Clinical Trial Team
- •Deliver medical oversight during study conduct
- •Present safety review and data interpretation conclusions to leadership
- •Represent the company as a medical expert in regulatory interactions
- •Engage with external experts and committees
- •Address EC/IRB and Health Authority questions
- •Support communication and publication planning
- •Conduct literature reviews and prepare position papers
- •Provide medical training to internal teams
Languages
English – Business Fluent
Benefits
Competitive Pay
- •Competitive salary
Additional Allowances
- •Generous social benefits
Career Advancement
- •Exciting opportunities for development
Other Benefits
- •Professional growth
- •Solution-oriented environment
Informal Culture
- •Collaborative environment
- •Multicultural environment
Startup Environment
- •Innovative culture
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Clinical Project/Trial Physician(m/w/x)
The AI Job Search Engine
Description
In this role, you will provide medical leadership and oversight for clinical projects, ensuring high-quality scientific input and guiding the Clinical Trial Team. Your day-to-day responsibilities will involve engaging with external experts, conducting safety reviews, and contributing to strategic decisions.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical degree (MD)
- •At least 5 years of experience in Clinical Development within the pharmaceutical or biotech industry
- •Clinical research or clinical practice experience in CNS and in at least one therapeutic area: Cardiovascular, Immunology, or Rheumatology
- •Strong knowledge of drug development and clinical trial process
- •Direct experience interacting with Health Authorities and understanding of regulatory requirements and ICH guidelines
- •Excellent written and spoken English skills
- •Strong organizational abilities
- •Proven success in complex matrix organizations and engaging with stakeholders
- •Hands-on, results-driven mindset with urgency and accountability
- •Proactive, solution-oriented approach
- •Analytical, data-driven thinker with attention to detail
- •Shares expertise openly and contributes to collaborative learning
- •Ability to think globally and understand broader strategic context
Education
Work Experience
5 years
Tasks
- •Provide medical leadership for assigned projects
- •Lead and oversee medical components of clinical projects
- •Ensure high-quality medical input into clinical documents
- •Contribute evidence-based insights to global clinical strategy
- •Offer medical and scientific guidance to the Clinical Trial Team
- •Deliver medical oversight during study conduct
- •Present safety review and data interpretation conclusions to leadership
- •Represent the company as a medical expert in regulatory interactions
- •Engage with external experts and committees
- •Address EC/IRB and Health Authority questions
- •Support communication and publication planning
- •Conduct literature reviews and prepare position papers
- •Provide medical training to internal teams
Languages
English – Business Fluent
Benefits
Competitive Pay
- •Competitive salary
Additional Allowances
- •Generous social benefits
Career Advancement
- •Exciting opportunities for development
Other Benefits
- •Professional growth
- •Solution-oriented environment
Informal Culture
- •Collaborative environment
- •Multicultural environment
Startup Environment
- •Innovative culture
About the Company
Idorsia Pharmaceuticals Ltd
Industry
Pharmaceuticals
Description
Idorsia is a biopharmaceutical company focused on discovering, developing, and commercializing transformative medicines.
- Novartis
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Global Program Safety Lead(m/w/x)
Full-timeOn-siteSeniorBasel - 1201 F. Hoffmann-La Roche AG
Medical Director — Multiple Sclerosis(m/w/x)
Full-timeOn-siteSeniorBasel - 1201 F. Hoffmann-La Roche AG
Lead Medical Director CVRM/Heart Failure(m/w/x)
Full-timeOn-siteSeniorBasel - 1201 F. Hoffmann-La Roche AG
Clinical Scientist immunology(m/w/x)
Full-timeOn-siteSeniorBasel