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Director, Translational Pharmacology and Discovery Medicine. Biopharm R&D.
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Director, Translational Pharmacology and Discovery Medicine. Biopharm R&D. : GlaxoSmithKline
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| Job Number |
54448 |
| Employee Type |
Full Time |
| Company Name |
GlaxoSmithKline |
| Location |
Stevange
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| Salary (year) |
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| Experience |
2 to 5 Years |
| Start Date |
6/19/2009 |
| Industry |
Pharmaceutical |
| Job Type |
Clinical |
| Relocation |
Not Required |
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| Apply online at company website |
| Description |
Basic Qualification
• Broad experience in early phase clinical trials
• Evidence of innovation in clinical trial design
• Broad understanding of the principles of Translational Pharmacology
• Strong integration and problem solving ability
• Broad pharmaceutical experience
• Strong knowledge of both basic and clinical science
• A strategic scientific mind
• Strong matrix skills
• MD and/or PhD required
Details
Description: Key member of a single integrated group that incorporates Translational Pharmacology and Discovery Medicine. . In addition, he/she will accountable for the integration of biology, pharmacology, clinical immunology and clinical pharmacology expertise into the development of assets with the objective of guiding Biopharm Unit assets from identification to first clinical use and beyond. This, with an in-depth understanding of the biology, clinical pharmacology and therapeutic potential of each asset.
Responsibilities:
• Integrating the Biopharm Unit TPDM activities through to C2MD
• Responsible for C2MD strategy for assets they are involved with
• Ensure an integrated package at every key milestone, to include asset, assay and differential pathway of development
• Build in, where appropriate, ability to transition earlier based on proof of pharmacology in pre-clinical and clinical areas
• Build in early pharmacology-based differentiation strategy and competitor evaluation input from appropriate group
• Build increased confidence in mechanism at every milestone
• Improve biology packages with a clear linkage from bench to bedside
• Increased communication among the various groups in Biopharm Research and its key business partners
• An integrated pharmacology and clinical pharmacology package to design pre-clinical experiments that lead to clinical utility
• The development of Clinical Plans for phases I and IIa studies in partnership with the therapeutic CEDD and for the design of studies such that the interpretation of preclinical and clinical data and selection of doses are specifically tailored to biopharmaceuticals.
• Ensure clinical regulation input related to pre-C2MD biopharmaceuticals.
• Ensure biopharmaceutical safety assessment input
• Accountable for liaising with VP Clinical Development regarding medical governance issues
• Responsible for the recruitment, motivation and the effective development of people in Translational Pharmacology and Discovery Medicine |
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| Requirements |
Preferred Qualification
Proven ability to use a combination of preclinical and clinical experience and apply a strong scientific rationale to clinical development, and in particular for early profiling of preclinical and clinical candidates and for obtaining early proof of mechanism/concept. |
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