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Observational Research Jobs (NOW HIRING)

Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report ...

Lead Epidemiology & Observational Research Strategy * Lead the design and execution of prospective observational studies, registries, and retrospective database studies across the early cancer ...

Learn and apply the Truveta data model, research platform, and analytic tools to conduct observational research studies. * Reproduce published clinical studies across multiple therapeutic areas (e.g ...

Learn and apply the Truveta data model, research platform, and analytic tools to conduct observational research studies. * Reproduce published clinical studies across multiple therapeutic areas (e.g ...

Experience in the design, execution, and analysis of observational research * Creative intelligence, including a willingness to develop new methodologies that take advantage of a modern real-world ...

Experience in the design, execution, and analysis of observational research * Creative intelligence, including a willingness to develop new methodologies that take advantage of a modern real-world ...

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Observational Research information

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How much do observational research jobs pay per hour?

As of May 30, 2026, the average hourly pay for observational research in the United States is $22.22, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $23.80 per hour, depending on experience, location, and employer.

What does an Observational Research job involve?

An Observational Research job involves studying behaviors, patterns, or outcomes without direct intervention, often in real-world settings. Researchers analyze data from sources like surveys, medical records, or natural environments to identify trends and insights. This role is commonly found in healthcare, social sciences, and market research. Strong analytical skills, attention to detail, and proficiency in statistical tools are typically required.

What are the key skills and qualifications needed to thrive in the Observational Research position, and why are they important?

To thrive in Observational Research, you need strong analytical skills, a background in epidemiology or public health, and experience in designing and conducting real-world data studies. Familiarity with statistical software such as SAS or R, as well as certifications like Certified Clinical Research Professional (CCRP), are commonly required. Attention to detail, critical thinking, and effective communication enable successful collaboration with multidisciplinary teams. These skills are critical for ensuring accurate data collection, meaningful analysis, and impactful contributions to scientific and healthcare advancements.

What are the typical daily responsibilities of an Observational Research professional?

As an Observational Research professional, your daily responsibilities often include designing study protocols, collecting and analyzing real-world data, and ensuring data quality and compliance with regulatory standards. You may work closely with clinical teams, biostatisticians, and project managers to interpret findings and present results. Collaboration across departments and communication with external partners, such as academic institutions or healthcare providers, are also common. This role may require literature reviews, preparing study documentation, and contributing to publication efforts, offering a diverse and intellectually stimulating work environment.
What are the most commonly searched types of Observational Research jobs? The most popular types of Observational Research jobs are:
What states have the most Observational Research jobs? States with the most job openings for Observational Research jobs include:
What job categories do people searching Observational Research jobs look for? The top searched job categories for Observational Research jobs are:
Infographic showing various Observational Research job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 40% Physical, and 60% Hybrid job distribution, with an average salary of $46,222 per year, or $22.2 per hour.
Senior Epidemiologist, Inflammation, IBD (FSP Sponsor Dedicated)

Senior Epidemiologist, Inflammation, IBD (FSP Sponsor Dedicated)

IQVIA, Inc.

Durham, NC • On-site

Full-time

Posted 15 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

54th of 203 rated it services


Job description

Location: Remote, candidates must be US-based
Join IQVIA's Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA's global expertise.
Core Function Description:
Design and conduct epidemiological studies to generate real-world 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 post-authorization studies. Skill sets of the Epidemiologist role are similarly required, with the expectation of more experience, able to operate strategically under limited supervision, well versed in current Epidemiology research methods, deep understanding of how RWE fits within drug development, regulatory, medical, safety and other functions.
Required Experience
  • Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE.
  • Lead, design, and manage epidemiological, biomarker and/or data science projects.
  • Lead, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries).
  • Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.
  • Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed.
  • 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.
  • Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
  • Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.

Technical Expertise:
  • Observational research methods (both Primary and Secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes.
  • Ability to design studies independently, (i.e., ability to translate research questions to create study design).

Subject Matter Expertise:
  • Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, PRO/COA, registry data) for methodologic research questions.
  • Deep, hands-on familiarity with EHR data curation behind health system firewalls, including practical knowledge of where key clinical outcomes are captured across data tables.
  • Expert knowledge and extensive experience with pharmacoepi methods (i.e., signal detection and validation methods).
  • Leverage RWE expertise to identify evidence gaps and develop options to address the evidence gaps in support of Clinical Development Programs.

Minimum Qualifications
  • PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master's degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.
  • Deep 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.
  • Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases.
  • 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 cross- functional collaborations in a matrix environment.
  • Ability to manage priorities and performance targets.
  • Experience in leading drug development project for 2+ years for therapeutic area of assignment preferred.

What's in it for you?
  • Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.
  • Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.
  • Access IQVIA's global network who supports your growth.

This is your chance to make an impact, while building a career that matters.
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 https://jobs.iqvia.com
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. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $110,500.00 - $276,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). 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.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US