Company Mission:
Job Purpose: The Chiesi - Regulatory Affairs internship will be an immersive experience that will include exposure to several regulatory projects directly related to the development of drugs and biologics. Education and training may include some FDA and Industry Sponsored lectures, but the focus will be a mainly on-the-job training experience.
Summary of Key Responsibilities:
80%
Global Regulatory Affairs Project Coordination:
20%
Additional Responsibilities:
100%
Required Skills:
Key Competencies:
Organizational Ability – Attention to timelines and deadlines. An ability to review and prioritize organizational commitments to maximize productivity across functional groups
Attention to Detail – Is thorough when performing work; conscientious about attending to detail; few errors in work performed; uses logical thinking that is well organized and methodical.
High Productivity – Produces consistent, high quality and quantity of outputs and meaningful results that contribute to the agency mission and strategic goal. Is efficient in producing results that are delivered on time or before. Able to multi-task productively because is well-organized; applies time management processes and procedures effectively
Teamwork/Collaboration – Works toward common goals by supporting, encouraging, and sharing information with colleagues, both internal and external
Communication — Speaks, writes, listens, and presents information in a logical and articulate manner appropriate for the audience.
Intern, Regulatory Affairs, US Global Rare Diseases • Cary, NC
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