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Director Clinical Development (Pazopanib PPL)
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Director Clinical Development (Pazopanib PPL) : MedImmune
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| Job Number |
57193 |
| Employee Type |
Full Time |
| Company Name |
MedImmune |
| Location |
collegeville
Pennsylvania
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| Salary (year) |
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| Experience |
2 to 5 Years |
| Start Date |
12/23/2009 |
| Industry |
Pharmaceutical |
| Job Type |
Clinical |
| Relocation |
Not Required |
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MedImmune
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| Description |
Basic Qualification
Medical Degree (MD) with certification in medical oncology, pediatric oncology or hematology.
Details
Responsible for the development implementation and management of the Clinical strategy for an Oncology asset.
Work within R&D matrix team to identify tumor types of interest from a medical and strategic perspective and oversee the development, conduct and evaluation of clinical studies to ensure global regulatory approval. |
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| Requirements |
Preferred Qualification
Significant drug development experience or related academic experience with experience in the conduct of Phase III clinical trials.
Strong leadership abilities and excellent presentation skills
Team oriented with experience managing in a global matrix environment
Excellent understanding of current medical oncology standards of care and areas of unmet need, and the willingness and ability to learn new areas of oncology.
Demonstrates highly developed multi-tasking skills, ability to prioritize tasks and deliver on deadlines, with high performance standards.
Demonstrated track record of quality decision making and creative problem resolution that impacts program /project direction.
Able to provide leadership in medical governance to include study design, protocol writing, evaluation of safety, adverse experience reporting and medical aspects of study conduct in both Clinical Development and Medical Affairs.
Responsible for developing and motivating the medical team in the development of product strategy, design, and implementation of global medical programs to support those strategies.
Ability to interpret clinical and efficacy data, including the strengths and weaknesses of study design and the applications of results to standard of care and clinical practice.
Provides assistance and advice to the Vice President and other senior staff through representation at senior level meetings and provision of clinical, regulatory and managerial leadership.
Support marketing activities – pre-launch publications, conferences, advisory boards.
Work with indication teams (strategy) and study teams (study design, implementation and conduct) to ensure regional alignment.
Key liaison with internal marketing partners, regulatory agencies and external opinion leaders.
Demonstrated track record of developing contacts with external consultants and opinion leaders. Ensures GSK’s strong reputation in the external community.
Demonstrated ability to listen and understand multidisciplinary points of view and work effectively in a team with both internal and external stakeholders
Excellent written and oral communication and communication skills. |
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