Research & Development Jobs at Jazz Pharmaceuticals
Found 4 Research & Development jobs in Pennsylvania at Jazz Pharmaceuticals
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Director, Clinical Development, Hematology/Oncology (Remote)
- Req ID:
- R010047
- Location:
- Philadelphia, PA -- [Remote/Home-Based]
- Category:
- Research & Development
Overview Jazz Pharmaceuticals is an international biopharmaceutical company focused on improving patients’ lives by identifying, developing and commercializing meaningful products that address unmet medical needs. We are continuing to expand our commercial product portfolio and our research and development pipeline in therapeutic areas that can leverage our unique expertise. Our …
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Director of Clinical Development, Oncology
- Req ID:
- R009522
- Location:
- Philadelphia, PA -- [Remote/Home-Based]
- Category:
- Research & Development
Brief Description: Jazz Pharmaceuticals is seeking a clinical development physician to join a team in hematology oncology drug development. You will be responsible for development of clinical studies, the oversight and interpretation of clinical trials data, clinical interactions with multidisciplinary groups across the company including R&D, commercial, regulatory, and business …
ViewDirector of Clinical Development, OncologyJob -
Senior Director, Clinical Development, Oncology (Remote)
- Req ID:
- R010059
- Location:
- Philadelphia, PA -- [Remote/Home-Based]
- Category:
- Research & Development
Brief Description : The Senior Director, Clinical Development, Oncology will play a key role in the development of Jazz’s Oncology pipeline with a particular focus on solid tumor Oncology assets and programs. The Senior Director, Clinical Development, Oncology will be involved in protocol development, protocol review, trial and study design …
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Senior Manager, Medical Writing (Remote)
- Req ID:
- R010171
- Location:
- Philadelphia, PA -- [Remote/Home-Based]
- Category:
- Research & Development
Brief Description: The Senior Manager Medical Writing is responsible for authoring and overseeing the completion of a broad range of complex documents in support of company products and projects. This individual will work with a cross functional study team to author high quality, submission ready documents. This individual will have …
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