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Salary
$74k – $201k per year (Estimated)
Location
In office (Singapore)
Seniority
Principal · 3+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

Essential Functions

  • Maintain Lab directory of service and associated global test codes. Support regional cost sheets and price sheets.
  • Maintain strong internal and external relationships, including global pathologists.
  • Management, oversight and coordination of the transition of clinical trials tests from development into global operations.
  • Ensure reliable, secure global procedures are developed, maintained and documented for new tests being implemented.
  • Supports Scientific Affairs and Sales in the acquisition of new testing
  • Review and approve quality control reports used to assess the validity of testing procedure, initiate remedial/corrective action where indicated.
  • Supports Sales in bid preparation and defense.
  • Provide clear and timely communications lines with Test Development, Scientific Affairs, Project Management, Pharmaceutical sponsors, laboratory operations, and investigators to ensure global services are developed and appropriate with all regulatory and customer requirements.
  • Develop a good understanding of the Q2 Solutions business and build relationships with global scientists and global laboratory operations.
  • Provide oversight to ensure reliable secure global technical and operational procedures are in place and provide support for improvement opportunities globally.
  • Remain aware of scientific and other advances, as the subject matter expert for assigned Lab services. Develop and maintain skills and knowledge appropriate to the post by undertaking training and attending meetings and conferences.
  • Ensures that safety, environmental, company and departmental policies and procedures are disseminated, understood, complied with and documented.
  • Ensure that employees receive appropriate training in working practices in line with local regulatory bodies.
  • All associates will be familiar with the safety, environmental rules and procedures applying to their job and take reasonable care for their own safety and that of other people.
  • Understand and apply the site Safety, Environmental Policy, Safety Management System and relevant legal safety & Environmental requirements

Qualifications

  • Bachelor's Degree equivalent combination of education, training and experience

Requirements

  • 3-5 years relevant industry experience
  • Deep scientific knowledge/experience with the ability to troubleshoot, guide and provide direction/performance management of staff as well have an understanding of operating budget and impacts to overall P&L. Skilled in extracting data to measure KPI's; Strong knowledge of relevant procedures, processes, and regulations; Working knowledge of department systems (i.e. QLIMS, NewLIMS, QNET); Strong knowledge of lab safety; Proficient in Microsoft Office

Q² Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. https://q2labsolutions.com/careers

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