IQVIA Solutions/ Pharmacovigilance & Risk Management Technology Solutions/ Sr Consultant/ System Implementation (R1089575) in Tokyo, JP at IQVIA™

Date Posted: 2/10/2020

Job Snapshot

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

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.

Role Definition

Involve in configuration of Pharmacovigilance / Drug Safety Adverse Event Reporting Systems at Pharmaceutical companies which includes understanding Business and Functional requirements, prepare design strategy, develop and implement optimized solutions using prototyping and POC techniques where required.

Job Duties

Key components of the responsibilities are as mentioned below:

• Provide application configuration expertise on Adverse Event Reporting products including, but not limited to Argus Safety, ARISg/j and related modules

• Requirements gathering and analysis

• Development and accountability of document deliverables (Requirement Documents CBD/CS UDDs SCR Verification IQs etc.)

• Design, build and implement configuration for clients

• Conduct POCs to understand the effectiveness of the solution; incorporate feedback into the solution

• Closely work with clients to support implementation and resolve issues

• Implement Quality measures to drive operational efficiencies and articulate the value to the customer

• Closely work with internal teams to support with the implementation and other tasks

• Communicate in both English and Japanese on projects needing bilingual support

Education & Other Qualifications

• BE/ME/MCA/MCS/MSc degree from reputed Institute/University


• 6-9 years of professional experience and strong knowledge with real time experience in Drug Safety Products from Oracle/Aris Global – Argus/ARISg/j

• Implementation/Upgrade/Maintenance of Drug Safety Application

• Working knowledge of writing SQL queries and/or PL/SQL code

• Experience in handling a team

• Excellent communication and inter-personal skills

• Ability to multi-task and work well under pressure

• Commitment to excellence and high quality standards

• Versatility, flexibility, and a willingness to work within changing priorities

• International travel readiness, work hours that overlap global client location Time-zones

• Business to native level of English and Japanese writing/speaking capability

Nice to Have Skills

• Working experience on associated modules like AgExchange/ESM, Percieve, or other Drug Safety Products

• Experience in Customizing E2B profiles

• Experience in configuring Aggregate and Periodic reports

• Knowledge of regulatory guidelines from the Food and Drug Administration (FDA), EMA and PMDA

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: R1089575