FSP Epidemiologist (Inflammation)

Location: Remote candidates must be USbased

Description:

• Design and conduct epidemiological studies to generate realworld evidence within time budget and quality standards including but not limited to: natural history of disease population characterization assessment of treatment patterns and unmet need development of external comparators benchmarking of clinical outcomes comparative safety and effectiveness research and postauthorization studies
• Support development of study protocols analysis plans and study reports to answer methodologic questions of priority to RWE
• Support the identification of fitforpurpose data for the timely execution of the RWE strategy
• Construct cohorts using RWD sources (e.g. claims EHR) and evaluate key variables including diagnosis and procedures codes and plan validation studies as needed
• Conduct analyses for descriptive and comparative research using RWD for methodologic research questions
• Contribute to the communication of observational research results and methods including development of pertinent sections of regulatory documents reports publications white papers.
• Support the effective communication of study/analysis results to support internal and external decisions
• Contribute to the development of processes and training aimed at increasing the efficiency quality and impact of functional activities
• Coauthor abstracts and manuscripts for external dissemination of methodologic study results
• Demonstrated ability to manage stakeholders including external vendors and internal crossfunctional teams

Minimum Requirements:

• PhD in Epidemiology or related field with a minimum of two (2) years of relevant postdoctoral experience preferably in pharmaceutical industry biotechnology or consulting environment. Masters degree in epidemiology or relevant scientific field plus five (5) years of experience in lieu of PhD may be acceptable.
• Understanding of observational research methods and experience to support the design and conduct of observational research including protocol statistical analysis plan and study report development
• Knowledge of secondary data sources and experience with secondary data analysis including electronic medical record and/or medical claims databases
  • Specifically experience working with commercially available US datasets and data platforms
  • Experience with OMOP datasets is desirable
• Background in chronic autoimmune inflammatory conditions such as Rheumatoid arthritis atomic dermatitis lupus and asthma is preferred
• A record of scientific publications demonstrating expertise in observational study design analysis and interpretation is preferred
• Demonstrated ability to function with an increasing level of autonomy and to develop productive crossfunctional collaborations in a matrix environment
• Ability to manage priorities and performance targets

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $110500.00 $276100.00. The actual base pay offered may vary based on a number of factors including jobrelated qualifications such as knowledge skills education and experience; location; and/or schedule (full or parttime). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.