Auto req 21033BR
Job Posting Title Pathologist Director - Comparative Biology & Safety Sciences, Thousand Oaks, CA or Seattle, WA
Career Category Preclinical Development
Employee Subgroup Salaried FT
Country (State/Region) United States - california
Location (City) US - CA - Thousand Oaks
Amgen Job Description This job can be based in Thousand Oaks, CA or Seattle, WA
Amgen is seeking an experienced toxicologic pathologist and drug development scientist to actively contribute to the drug development process from target selection and lead optimization through product registration. Working in a collaborative team environment with other colleagues in Research and Translational Sciences (e.g. therapeutic area scientists, drug metabolism, chemistry, protein sciences, early clinical development), the incumbent will contribute to the selection and safety assessment of small molecule and biologic therapeutics and represent Comparative Biology & Safety Sciences (CBSS) on drug development teams within Amgen. Amgen scientists make significant contributions, work in multiple therapeutic areas, and mentor and motivate their colleagues. Scientific excellence, curiosity, proactivity, critical thinking and review are part of our working principles.
As a Pathologist Director in CBSS, you will design, implement, analyze and integrate a wide range of datasets from nonclinical safety and investigative studies and programs in support of drug discovery and development. Experience in resolving nonclinical safety issues through the establishment of novel protocols to solve experimental questions, in addition to devising strategies and planning activities to achieve project goals is required. An understanding of innovative science and technology employed to enhance investigation of drug development safety liabilities is needed. Part of your role will be as a CBSS Lead, actively participating and contributing to project teams and providing regular updates as appropriate to senior management. You will be asked to mentor other colleagues and to contribute your expertise in the peer-review of plans and work products emerging from the department.
Basic Qualifications â ¢ D.V.M. and Ph.D. degrees & 4 years of directly related experience.
â ¢ Board certification in anatomic veterinary pathology.
Preferred Qualifications â ¢ Ph.D. in a biological science with expertise in a specific disease discipline, comparative medicine or pathology highly preferred.
â ¢ A minimum of a combined 8 years experience of academic and industry experience in nonclinical drug development/pathology demonstrating a sustained record of achievement.
â ¢ Experience as a nonclinical safety representative on a drug development project team
â ¢ Experience to critically evaluate and interpret integrated sets of data from scientific experiments and then translate the potential clinical impact.
â ¢ Excellent verbal and written communication skills are necessary as the incumbent will contribute to appropriate sections of regulatory documents.
â ¢ Leadership and influencing abilities including managing differences in opinion, prioritization skills, resilience, and the demonstration of achieving aims through proactivity and persuasion, especially in a team environment.
â ¢ A working knowledge of computational and database tools for assessing multi-dimensional data and an ability to effectively query the literature and other public domain data repositories.
â ¢ The ability to work independently and to build productive cross-functional collaborations both internally and externally.
Job Posting Title Pathologist Director - Comparative Biology & Safety Sciences, Thousand Oaks, CA or Seattle, WA
Career Category Preclinical Development
Employee Subgroup Salaried FT
Country (State/Region) United States - california
Location (City) US - CA - Thousand Oaks
Amgen Job Description This job can be based in Thousand Oaks, CA or Seattle, WA
Amgen is seeking an experienced toxicologic pathologist and drug development scientist to actively contribute to the drug development process from target selection and lead optimization through product registration. Working in a collaborative team environment with other colleagues in Research and Translational Sciences (e.g. therapeutic area scientists, drug metabolism, chemistry, protein sciences, early clinical development), the incumbent will contribute to the selection and safety assessment of small molecule and biologic therapeutics and represent Comparative Biology & Safety Sciences (CBSS) on drug development teams within Amgen. Amgen scientists make significant contributions, work in multiple therapeutic areas, and mentor and motivate their colleagues. Scientific excellence, curiosity, proactivity, critical thinking and review are part of our working principles.
As a Pathologist Director in CBSS, you will design, implement, analyze and integrate a wide range of datasets from nonclinical safety and investigative studies and programs in support of drug discovery and development. Experience in resolving nonclinical safety issues through the establishment of novel protocols to solve experimental questions, in addition to devising strategies and planning activities to achieve project goals is required. An understanding of innovative science and technology employed to enhance investigation of drug development safety liabilities is needed. Part of your role will be as a CBSS Lead, actively participating and contributing to project teams and providing regular updates as appropriate to senior management. You will be asked to mentor other colleagues and to contribute your expertise in the peer-review of plans and work products emerging from the department.
Basic Qualifications â ¢ D.V.M. and Ph.D. degrees & 4 years of directly related experience.
â ¢ Board certification in anatomic veterinary pathology.
Preferred Qualifications â ¢ Ph.D. in a biological science with expertise in a specific disease discipline, comparative medicine or pathology highly preferred.
â ¢ A minimum of a combined 8 years experience of academic and industry experience in nonclinical drug development/pathology demonstrating a sustained record of achievement.
â ¢ Experience as a nonclinical safety representative on a drug development project team
â ¢ Experience to critically evaluate and interpret integrated sets of data from scientific experiments and then translate the potential clinical impact.
â ¢ Excellent verbal and written communication skills are necessary as the incumbent will contribute to appropriate sections of regulatory documents.
â ¢ Leadership and influencing abilities including managing differences in opinion, prioritization skills, resilience, and the demonstration of achieving aims through proactivity and persuasion, especially in a team environment.
â ¢ A working knowledge of computational and database tools for assessing multi-dimensional data and an ability to effectively query the literature and other public domain data repositories.
â ¢ The ability to work independently and to build productive cross-functional collaborations both internally and externally.
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