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IQVIA

Runs drug trials and sells health data to pharma

Associate/Senior Outcomes Researcher - Multiple Teams

ConsultingConfirmed live in the last 24 hours
Full-timeSeoul, South KoreaNo salary listedIn-person

About the Job

Requirements

  • At least 3 years of experience in outcomes research using real-world data sources such as claims databases and hospital electronic medical record data, and generating real-world evidence.
  • A Master's degree or higher in Statistics, Epidemiology, Pharmacoepidemiology, Public Health, Health or Medical Informatics, or a related field, with demonstrated experience in real-world data-based research projects, publications, or scientific communications.
  • Working knowledge of at least one statistical programming language: SAS, R, or Python.
  • Understanding of the Korean healthcare system and pharmaceutical industry environment.
  • Demonstrable analytical, interpretative, and problem-solving skills.
  • Good English communication skills.

Responsibilities

  • Carry out work relating to health economics and outcomes research business areas, including database studies, longitudinal retrospective or prospective observational studies, cross-sectional surveys of patients, healthcare providers, or payers, and patient-reported outcomes research.
  • Work with supervision, independently, and/or as part of a project team on defined tasks.
  • Develop, review, implement, and execute prospective or retrospective outcomes research protocols, statistical analysis plans, and reports.
  • Source, search, collect, and generate local data; develop analysis plans and provide input to complex health economic models.
  • Participate in business development and internal initiatives, including partial proposal development based on client requests for proposals, internal knowledge sharing, and presentations to colleagues.
  • Manage projects and liaise with clients; attend client and external meetings and present research findings and analyses.
  • Draft, revise, submit, and present abstracts, posters, and manuscripts for publication and conference proceedings.

Desired Qualifications

  • Contribute to applying real-world data to post-marketing evidence generation, including risk management planning, safety evaluation, drug utilization assessment, and post-authorization evaluation of treatment effectiveness and safety in support of evolving regulatory requirements.
  • Contribute to multi-site real-world evidence studies using diverse real-world data sources, including hospital electronic medical record data, and support expansion of data partnerships and research networks through site onboarding, data governance, institutional review board/data review board strategies, and standardized analytical approaches.

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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