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TA Group Director – Clinical Pharmacology & Quantitative Pharmacology – Oncology
| Company | AstraZeneca |
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| Location | Gaithersburg, MD, USA |
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| Salary | $196868.8 – $295303.2 |
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| Type | Full-Time |
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| Degrees | Master’s, PharmD, PhD |
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| Experience Level | Expert or higher |
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Requirements
- Demonstrated broad translational and clinical development experience with a minimum of 10 years in international drug development (early and late clinical).
- Ability to develop people, drive performance, and hold self and others accountable.
- Proven record of building successful partnerships and collaborations with cultural sensitivity.
- Experience leading teams.
- Strong leadership capabilities including influencing skills.
- Experience in mentoring and developing others.
- Conceptual, analytical, and strategic thinking.
- International scientific reputation from publishing in quantitative clinical pharmacology.
- Ability to identify, develop, and execute strategic CPQP activities.
- Relevant TA disease domain knowledge.
- Relevant regulatory experience (written/oral).
- Knowledge of regulatory, compliance processes, standards, and issues specific to Clinical Pharmacology & Quantitative Pharmacology.
Responsibilities
- Lead a team delivering quality clinical pharmacology input from pre-CDID to life-cycle management.
- Collaborate with CPQP TA Head for resource management, enhancing productivity and cost efficiency.
- Support TA Head in strategy development, scientific operations, and business management.
- Act as delegate for TA Head in various meetings and interactions.
- Develop and implement clinical pharmacology strategies as project Clinical Pharmacologist.
- Cultivate a culture supportive of MIDD approaches across TA.
- Foster positive collaboration with key partner functions.
- Provide scientific and strategic input into development plans across TA.
- Oversee scientific modeling work in early and late development.
- Evaluate candidates for in/out-licensing.
- Lead peer reviews within and across TA.
- Mentor and contribute to learning development within TA.
- Monitor new methodologies and applications in the environment.
- Increase AZ profile externally through speaking engagements and publications.
- Ensure CPQP contributions align with regulations and compliance standards.
Preferred Qualifications
- PhD degree preferred or equivalent (M.Sc./Pharm.D.) with relevant experience required.
