Junior Regulatory and Start-Up Specialist (R1105451) in , Egypt at IQVIA™

Date Posted: 11/15/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    , Egypt
  • Experience:
    Not Specified
  • Date Posted:
    11/15/2019
  • Job ID:
    R1105451

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.

An English speaking with scientific background candidate is required for a junior Regulatory and Start-Up position (French language is a plus).

RESPONSIBILITIES

  • Assist the team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures.
  • Review documents for completeness, consistency and accuracy, under guidance of senior staff.
  • Prepare regulatory submission folders according to the scope of work and operating procedures.
  • May perform budget and contract negotiations on allocated projects or support senior staff.
  • Prepare client deliverable documents using appropriate tools and may draft text for straightforward documents, under guidance of senior staff.
  • Assist with completion of relevant systems, databases, tracking tools, timelines and project plans with project specific information.
  • Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers.
  • Interact with internal and external clients, under guidance of senior staff.
  • May perform IP release activities on small, straightforward projects or support reviews for larger projects.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • French, English and Arabic fluency.
  • Good interpersonal communication and organizational skills.
  • Good word processing skills and knowledge of MS Office applications.
  • Good attention to detail.
  • General awareness clinical trial environment and drug development process.
  • Ability to work on multiple projects.
  • Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.

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: R1105451