Regulatory Affairs TALENT POOL

Description

• Gain exceptional professional knowledge about Regulatory Submission, Clinical Trial and related Regulatory Operation areas to support our teams
• Help to build a knowledge base and leverage best practices in the area of Regulatory Submissions, Clinical Trials and supporting activities
• Develop your mentoring skills by training new joiners or other team members
• Continuously improve process efficiency and support service quality exercises
• Build a wide network within the operation groups to ensuring smooth operations in different teams

Qualifications

• 1-3 years of related experience in a similar role, preferably with a life sciences degree and/or data/system related degree
• Proficiency in a broad range of IT skills, including expert-level use of Word, Excel and Acrobat and experience with document-management systems (e.g., Documentum) and document-sharing systems (e.g., SharePoint)
• Maintain and manage regulatory documents and data in regulatory information management systems (e.g RIM, Documentum) and/or document-sharing systems (e.g., SharePoint)
• Tenacious attention to detail and consistency, especially with respect to data, style, format, and layout and ability to format technical documents using electronic tools (e.g., Acrobat)
• The skills for collaboration and the ability to interface effectively with submission leads and colleagues located in other countries.
• Ability to work in fast-paced global teams
• Fluent in written and spoken English
• Logical thinking and/or process analyst mentality