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IQVIA

Runs drug trials and sells health data to pharma

Associate Principal Scientist - Lab Operations, Flow Cytometry

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSingaporeNo salary listedIn-person

About the Job

Requirements

  • A Bachelor's degree or equivalent combination of education, training, and experience is required.
  • Three to five years of relevant industry experience is required.
  • Deep scientific knowledge and experience, including the ability to troubleshoot, guide, and provide direction and performance management of staff.
  • An understanding of operating budgets and their impacts on overall profit and loss is required.
  • Skill in extracting data to measure key performance indicators is required.
  • Strong knowledge of relevant procedures, processes, and regulations is required.
  • Working knowledge of department systems, including QLIMS, NewLIMS, and QNET, is required.
  • Strong knowledge of laboratory safety is required.
  • Proficiency in Microsoft Office is required.

Responsibilities

  • Maintain the laboratory directory of services and associated global test codes, and support regional cost sheets and price sheets.
  • Maintain strong internal and external relationships, including with global pathologists.
  • Manage, oversee, and coordinate the transition of clinical trial tests from development into global operations.
  • Ensure reliable, secure global procedures are developed, maintained, and documented for new tests being implemented.
  • Support Scientific Affairs and Sales in acquiring new testing services.
  • Review and approve quality control reports used to assess the validity of testing procedures, and initiate remedial or corrective action where indicated.
  • Support Sales in bid preparation and defense.
  • Communicate clearly and promptly with Test Development, Scientific Affairs, Project Management, pharmaceutical sponsors, laboratory operations, and investigators to ensure global services are developed appropriately and meet regulatory and customer requirements.
  • Develop an 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 support global improvement opportunities.
  • Remain aware of scientific and other advances as the subject matter expert for assigned laboratory services.
  • Maintain skills and knowledge appropriate to the post through training and attendance at meetings and conferences.
  • Ensure safety, environmental, company, and departmental policies and procedures are disseminated, understood, followed, and documented.
  • Ensure employees receive appropriate training in working practices in line with local regulatory bodies.
  • Become familiar with the safety and environmental rules and procedures applicable to the job, and take reasonable care for personal safety and the safety of others.
  • Understand and apply the site Safety and Environmental Policy, Safety Management System, and relevant legal safety and environmental requirements.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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