-
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
-
and regulatory operations and environment in countries under responsibility English is required. Prior Experience Demonstrated clinical research experience and/or study management/startup project
-
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
-
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
-
. High attention to detail. Ability to consolidate comments from multiple sources (e.g., emails, meeting minutes). NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Ability to flex working
-
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
-
collaboratively in a laboratory environment PREFERRED QUALIIFICATIONS Experience in formulation and manufacturing of SDDs targeted at bioavailability enhancement Experience in breaking down and isolating
-
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
-
skills to track numerous tasks for multiple simultaneous projects in a deadline-oriented environment Direct external vendors and manage budgets, timelines, and quality of deliverables PREFERRED
-
skills to track numerous tasks for multiple simultaneous projects in a deadline-oriented environment Direct external vendors and manage budgets, timelines, and quality of deliverables PREFERRED