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Project Toxicologist with large molecule experience(m/w/x)
Steering non-clinical safety evaluations for in-licensing opportunities and new medicine development at a global pharmaceutical company. PhD or DVM, plus 10+ years in biopharmaceutical development required. Global project team collaboration, cross-functional interaction.
Requirements
- PhD, DVM, or equivalent
- Minimum 10 years of experience in large molecule development
- Ability to manage scientific issues and multiple projects
- Board certification such as DABT (advantageous)
- Effective communication to key stakeholders
- Experience in a matrixed team environment
- Strong organizational and interpersonal skills
- Influencing through effective communication
- Passion for mentoring junior colleagues
Tasks
- Develop and execute a nonclinical safety strategy
- Represent Pharmaceutical Sciences in global project teams
- Contribute to the selection and development of new medicines
- Interact closely with discovery therapeutic areas and regulatory functions
- Steer non-clinical safety evaluations for in-licensing opportunities
- Represent non-clinical safety in collaborations with external partners
- Generate concise safety assessments for internal decision-making
- Prepare regulatory submission documentation for health authority reviews
- Lead a team of experts during critical project stages
- Utilize interpersonal skills to navigate a highly matrixed environment
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
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Project Toxicologist with large molecule experience(m/w/x)
Steering non-clinical safety evaluations for in-licensing opportunities and new medicine development at a global pharmaceutical company. PhD or DVM, plus 10+ years in biopharmaceutical development required. Global project team collaboration, cross-functional interaction.
Requirements
- PhD, DVM, or equivalent
- Minimum 10 years of experience in large molecule development
- Ability to manage scientific issues and multiple projects
- Board certification such as DABT (advantageous)
- Effective communication to key stakeholders
- Experience in a matrixed team environment
- Strong organizational and interpersonal skills
- Influencing through effective communication
- Passion for mentoring junior colleagues
Tasks
- Develop and execute a nonclinical safety strategy
- Represent Pharmaceutical Sciences in global project teams
- Contribute to the selection and development of new medicines
- Interact closely with discovery therapeutic areas and regulatory functions
- Steer non-clinical safety evaluations for in-licensing opportunities
- Represent non-clinical safety in collaborations with external partners
- Generate concise safety assessments for internal decision-making
- Prepare regulatory submission documentation for health authority reviews
- Lead a team of experts during critical project stages
- Utilize interpersonal skills to navigate a highly matrixed environment
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
About the Company
1201 F. Hoffmann-La Roche AG
Industry
Pharmaceuticals
Description
Roche is dedicated to advancing science and ensuring access to healthcare for everyone, with over 100,000 employees globally.
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