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to inspection activities and regulatory agency questions. QUALIFICATIONS / SKILLS Education/Experience: Minimum 4+ years experience in regulated environment, or equivalent practical experience (pharmaceutical
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documents Facilitate team and cross functional meetings. Education Qualifications: Bachelor's degree in a science or life sciences required 3+ years experience in a regulated environment; pharmaceutical
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OR ENVIRONMENT REQUIREMENTS Some travel (~5%) across GPD sites for face to face meetings, if necessary. Depending on location may need to accommodate global teleconference calls across different time zones. Work
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and regulatory operations and environment in countries under responsibility English is required. Prior Experience Demonstrated clinical research experience and/or study management/startup project
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SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Occasional travel may be required. Relocation support available Work Location Assignment:On Premise The annual base salary for this position ranges from
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enhancement opportunities and quality improvements in the different R&D activity areas. Additional responsibilities include ongoing assessment and identification of external environment trends/best practices as
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as appropriate. PREFERRED QUALIFICATIONS Advanced degree (MS/MA) is preferred. Knowledge of data and/or document anonymization strongly preferred. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT
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deadlines Creativity, resourcefulness, high energy and flexibility Excellent verbal and written communication skills. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Ability to travel 25
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in a collaborative environment with other units involved in clinical research. This position is being recruited in the following faculty titles, designation into the following title series will be
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and project/program issues and risks and drives resolution through a matrix environment, effectively documenting decisions/rationale. Partners with the Product Team Leader to prioritize asset level