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Regulatory Affairs Officer 1 - (1712164) in Tokyo, JP at IQVIA™

Date Posted: 3/11/2018

Job Snapshot

  • Employee Type:
  • Location:
    Tokyo, JP
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

IQVIA™ is a leading integrated information and technology-enabled worldwide healthcare service provider. Formed by the merger of Quintiles and IQVIA™ , we use our experience, resources and reputation to help our clients drive healthcare forward.A career at IQVIA™ will give you the opportunity to play an important part in helping our clients improve patient healthcare and make real medical breakthroughs.
• Acts as a Regulatory Team Leader on small, straightforward regulatory projects and/or becomes involved in a small single service project, under the guidance of senior staff. 
• Identifies project needs, tracks project timelines, implements client requests and manages day-to-day workload in collaboration with senior staff, as appropriate. 
• Prepares and/or reviews regulatory documentation in area of expertise, as appropriate. 
• Actively participates in project teams with internal and external customers independently and communicates confidently in straightforward matters. 
• Understands the Scope of Work, deliverables and management of budget for any given project. 
• May prepare slides and background material for small, straightforward business development meetings under senior guidance and present to clients at bid defence meetings by phone or in person. 
• May prepare and deliver training, as appropriate.
 • Performs other tasks or assignments, as delegated by Regulatory management. 
All responsibilities are essential job functions unless noted as nonessential (N). 

Job Requirements

EEO Minorities/Females/Protected Veterans/Disabled

• Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate 
 • Good, solid interpersonal communication (oral and written) and organisation skills 
 • Strong software and computer skills, including MS Office applications  
• Demonstrates self-motivation and enthusiasm 
 • Ability to work on several projects, with direction from senior staff as appropriate 
 • Ability to follow SOPs consistently; provides independent thought to assist in process improvements 
 • Ability to make decisions on discrete tasks under senior supervision 
 • Ability to establish and maintain effective working relationships with co-workers, managers and clients 

MINIMUM REQUIRED EDUCATION AND EXPERIENCE • Degree in life science-related discipline or professional equivalent plus at least 1 year relevant experience* or high school diploma plus at least 5-7 years experience* (*or combination of education, training and experience) 
You can drive your career at IQVIA™ and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.We invite you to join us on our exciting journey. Apply now.Help us make a difference in patient health.IQVIA™ is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.

Job ID: 1712164