Regional Regulatory Affairs Manager (R1092738) in Singapore, SG at IQVIA™

Date Posted: 9/14/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Singapore, SG
  • Experience:
    Not Specified
  • Date Posted:
    9/14/2019
  • Job ID:
    R1092738

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Responsibilities

  • Acts as a Lead Regulatory Professional on any type of writing or technical project, with limited guidance from senior staff using experience and initiative to generate new and unusual document types to meet customer requirements.
  • Provides strategic regulatory and/or technical consultancy on a variety of projects and provides senior review and guidance for most documents prepared by junior colleagues.
  • • May act as a Project Manager for a stand-alone project, with full project management responsibility.
  • May prepare a single service regulatory or technical proposal for senior review and/or propose budgets for less routine projects, out of scope activities and potential budget efficiencies. Deliver business development presentations to customers with confidence and detailed knowledge, as directed.
  • Independently meet with customers face to face to discuss project status. Identifies creative solutions to challenges that are acceptable to IQVIA and customers, thereby consistently receiving positive customer feedback.
  • Ensures compliance with regulatory processes, ensuring readiness for internal or external project audits.
  • May design training materials and deliver training externally and internally.
  • May represent region or site on a regulatory, technical or cross functional Initiative.
  • Performs other tasks or assignments, as delegated by Regulatory management.

Requirements

  • Degree in life science-related discipline or professional equivalent plus at least 5 years relevant experience, including 3 years of regulatory experience in the region (SEA)
  • Extensive experience in regulatory and/or technical writing in SEA region
  • Advanced negotiating and influencing skills and the ability to identify and resolve issues, using flexible adaptable approach. 
  • Strong software and computer skills, including MS Office applications    Sets a positive example to more junior colleagues relating to a professional manner, positive attitude and communication style with customers and colleagues   
  • May take calculated risks when making decisions, seeking guidance from Regulatory management, as appropriate; demonstrates autonomy and initiative, as appropriate   

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.



Job ID: R1092738