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Clinical Project Manager
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| Department: |
Clinical Development |
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| Date Posted: |
05/09/2008 |
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| Location: |
The Woodlands, TX |
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| Reference: |
CPM 23894 |
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Job Description: |
This position will be responsible for overseeing the daily activities of Phase 1-3 world-wide clinical trials of drug candidates by ensuring that high quality and valid data supports regulatory applications and approvals of new-marketed products and indications. Responsibilities will include, but will not be limited to: managing Clinical personnel to conduct investigator identification, selection, training and routine monitoring; maintaining and negotiating vendor contracts; managing budgets and payments; serving as the study lead on Clinical project teams; participating in the design and development of clinical study protocols and CRFs across a range of therapeutic areas to ensure monitoring efforts fully complement the drug development process within established timelines; managing and executing trials through a combination of internal and external (CRO) staff; and other duties as assigned or required. |
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| Qualifications: |
- Bachelor's or master's degree in a scientific related discipline
- Minimum of eight (8) years of clinical development experience in a pharmaceutical or clinical research organization
- Previous Clinical Project Manager experience in conducting and managing Phase 1-3 clinical trials
- Ability to manage multiple projects across several departments while influencing project decisions in coordination with clinical, regulatory, pre-clinical and CMC timelines
- Proficiency with Microsoft Office Suite
- Excellent organization and communication skills
- Ability and desire to work in a team-oriented environment
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Lexicon's Benefits
Lexicon Pharmaceuticals is an equal opportunity employer. |
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