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Clinical Development Manager, Life Cycle Management
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Clinical Development Manager, Life Cycle Management : GlaxoSmithKline
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| Job Number |
54418 |
| Employee Type |
Full Time |
| Company Name |
GlaxoSmithKline |
| Location |
Rixensart - Wavre (Belgium)
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| Salary (year) |
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| Experience |
2 to 5 Years |
| Start Date |
6/16/2009 |
| Industry |
Pharmaceutical |
| Job Type |
Clinical |
| Relocation |
Not Required |
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| Description |
Basic Qualification
Profile
• Medical Degree
• Fluent in English (written and spoken)
• Some previous experience of research (2 years)
• Experience in Clinical R & D is an added value
• Strong leadership potential
• A strong team spirit
• Customer-oriented mind
• Strong organisation skills, i.e. take a global view, respect of timings, and work with a sense of urgency
• Precision: detailed oriented, focus on data quality
• Ready to travel when required
Details
Job Purpose
To take full responsibility for Clinical Projects within the context of the GSK Biologicals process in order to ensure the high quality and delivery on time of all clinical data that will allow the world-wide registration in compliance with the clinical development plan, good clinical practices (GCP), and GSK Biologicals standard operating procedures (SOP)
Responsibilities
• Coordinate and manage the clinical development of one or more candidate vaccines, including selection of investigators, setting up of the development plan, design of clinical studies, analysis and data reporting and responsibility of the clinical report for registration.
• Coordinate of Clinical Project Team for the vaccine(s) in development.
• Provide scientific and medical support for the project team(s), the marketing teams and GSK LOUs (Local Operating Units).
• Be a Representative of the Clinical R&D Team within the project Team, eventually also with the health authorities and KOLs (Key Opinion Leaders) in the vaccine domain.
• Carry out, and/or help to write scientific articles, about GSK Biologcals activities in the vaccine domain.
• Maintain an objective and continuous ‘up and downstream’ communication of information relating to clinical activities within the vaccine domain.
• Manage budgets for clinical studies.
• Active control of timing and milestones in agreement with Management. |
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| Requirements |
Preferred Qualification
Profile
• Medical Degree
• Fluent in English (written and spoken)
• Some previous experience of research (2 years)
• Experience in Clinical R & D is an added value
• Strong leadership potential
• A strong team spirit
• Customer-oriented mind
• Strong organisation skills, i.e. take a global view, respect of timings, and work with a sense of urgency
• Precision: detailed oriented, focus on data quality
• Ready to travel when required |
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| Contact Info |
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Apply online at company website |
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