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and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate
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simultaneous projects in a deadline-oriented environment Direct external vendors and manage budgets, timelines, and quality of deliverables PREFERRED QUALIFICATIONS Experience in assigned therapeutic area NON
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and key external stakeholders through strong interpersonal skills Strong organizational skills to track numerous tasks for multiple simultaneous projects in a deadline-oriented environment Direct
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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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and investigators/medical professionals Is a team player, works well in a team environment both as a leader and a key contributor Has a global perspective and mindset, with the ability to work
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significant volume of projects developed in a field-based environment, while exhibiting the ability to prioritize, successfully implement, and demonstrate excellent judgment skills and work in a continuous
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significant volume of projects developed in a field-based environment, while exhibiting the ability to prioritize, successfully implement, and demonstrate excellent judgment skills and work in a continuous
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keeping and attention to detail. The ability to work in a fast-paced matrix-team environment. Strong verbal, written communication, and interpersonal skills. PREFERRED QUALIFICATIONS M.S. degree with 2
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collaboratively in a laboratory environment PREFERRED QUALIIFICATIONS Experience in formulation and manufacturing of SDDs targeted at bioavailability enhancement Experience in breaking down and isolating
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multidisciplinary team environment. Ensure appropriate use of animals in compliance with all regulatory requirements and internal standards. QUALIFICATIONS Must-Have Bachelor's degree with 6+ years relevant