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Associate. Director, HEOR

Pacira BioSciences, Inc.
United States, United Statesfull_timeVerifiedPosted 13 Jun 2024

About the role

About Pacira     Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.        Why work with us?     Rarely do you have an opportunity to do work that really matters. What drives us is our mission. What makes us successful are our people.  At Pacira, you are part of an inclusive culture that fosters collaboration, growth, and innovative thinking - a place where you can make an impact and help change the standard of care in non-opioid pain management. Be part of our movement, let’s pursue excellence together.Summary:
The Associate Director,
HEOR, is the major contributor and driver to the real-world patient health and economic outcome research in support of Pacira products. The Associate Director, HEOR, assists in all aspects of data-related activities in company-sponsored registries, including data collection, management, analysis, and report. Collaborating with the analytical team, the Associate Director performs programming in processing data at different levels, verifies analytical datasets, and applies conventional and novel statistical methods to summarize registry data and generate clinically meaningful results. The Associate Director also leads the development of dashboards which aid in an overview of the datasets (e.g., ongoing registry data) with display of distribution and descriptive statistics on data fields. Well-versed in secondary databases (e.g., administrative claims, EHR/EMR), the Associate Director conducts statistical analysis in health and economic outcome research using such databases. The Associate Director works closely with his/her manager to develop and design outcome studies. As needed, the Associate Director drafts statistical analysis plan to conduct data analyses. This position may interact with internal and external stakeholders to ensure appropriate communication of results.
 Essential Duties & Responsibilities:The following statements are intended to describe the general nature and level of work being performed by an individual assigned to this job. Other duties may be assigned. 
  • Program in data process, management, and statistical analysis on registry and large claims/EHR/EMR databases using SAS/SQL/R/Phyton, etc.
  • QC and verify derived data fields and analytical datasets created by team programmers.
  • Identify selection and application of optimal and appropriate statistical methods to health and economic outcome studies.
  • Develop dashboards for overview of selected databases (e.g., registries) using Tableau and other application tools.
  • Develop statistical analysis plan and statistical outputs to support internal business strategy and external communications.
  • Assist in publications of health and outcome research studies including drafting and reviewing sections of methods and results.
  • Assist in development of presentation material to internal and external stakeholders.
  • Maintain awareness of new statistical methods, tools, and data sources to ensure that projects represent current state of science, and maintains professional knowledge by reading scientific journals, attending internal and external courses, and undertaking methodological research.
 Supervisory Responsibilities:This position may have supervisory responsibilities. Interaction:The incumbent works with internal teams (corporate, medical, and sales), and vendors. Education and Experience:
  • A master’s degree or higher in epidemiology, biostatistics, psychometrics, or a closely related fields with at least 7 years of hands-on analytical and research experience is required
  • Statistical programming is required
  • Experience working with large administrative or medical records databases is required
  • Experience in statistical modeling of multivariable analysis, repeated measures, and specific data distribution to conduct clinical and outcome research is required
  • Experience with non-randomized designs is required
  • Experience with writing protocols in general and particularly the statistical m

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Company

Pacira BioSciences, Inc.

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