ZipRecruiter

Log In

1

Overnight Public Health Research Jobs (NOW HIRING)

Washington University of St. Louis

Routinely collects public health data under public health research protocols. * Performs other duties incidental to the work described herein. Working Conditions: Job Location/Working Conditions

Washington University of St. Louis

$23.63 - $35.49/hr

Location SAINT LOUIS, MO 63110 Scheduled Hours 20 Position Summary Assists investigators as coordinator of a basic to moderately complex public health research study; may be responsible for multiple ...

next page

Showing results 1-20

All Jobsovernight JobsScience JobsSocial Science JobsSocial Science Analyst JobsOvernight Public Health Research Jobs

Overnight Public Health Research information

See salary details

$64K

$96.7K

$117K

How much do overnight public health research jobs pay per year?

As of Aug 28, 2026, the average yearly pay for overnight public health research in the United States is $96,670.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $111,500.00 per year, depending on experience, location, and employer.

What is an overnight public health researcher?

An Overnight Public Health Researcher is a professional who conducts research and data analysis on public health issues during overnight hours. Their work often involves monitoring and responding to emerging health threats, collecting and analyzing data, and supporting ongoing studies that require round-the-clock attention. These researchers may work in laboratories, hospitals, public health agencies, or academic institutions. The overnight schedule ensures that critical research and surveillance activities continue without interruption, especially in settings where public health emergencies can arise at any time.

What are the key skills and qualifications needed to thrive as an overnight public health researcher?

To thrive as an Overnight Public Health Researcher, you need a background in public health, epidemiology, or a related field, often supported by a relevant degree. Familiarity with data analysis software (like SPSS or SAS), research databases, and compliance with IRB protocols is typically required. Strong attention to detail, time management, and the ability to work independently during non-standard hours are crucial soft skills. These competencies ensure accurate data collection, reliable research outcomes, and the ability to advance public health initiatives even during overnight shifts.

What are some common challenges faced by professionals working in overnight public health research roles?

Professionals in overnight public health research roles often encounter challenges such as adjusting to non-traditional work hours, which can impact sleep patterns and work-life balance. Additionally, they may have to manage limited onsite support and resources during nighttime shifts, requiring a high degree of independence and problem-solving. Effective communication with day-shift colleagues is essential to ensure continuity of research and data integrity. Despite these challenges, overnight roles can offer unique opportunities for focused work and may serve as a stepping stone to advanced research positions.

What is the difference between Overnight Public Health Research vs Public Health Data Analyst?

AspectOvernight Public Health ResearchPublic Health Data Analyst
CredentialsTypically requires a Master’s in Public Health or related field; research experienceBachelor’s or Master’s in Public Health, Statistics, or related field; data analysis skills
Work EnvironmentResearch labs, field sites, or academic settings, often with night shiftsOffice or remote settings, primarily during daytime hours
Employer & Industry UsageUniversities, government agencies, research institutionsPublic health departments, healthcare organizations, research firms

Overnight Public Health Research involves conducting research activities during night shifts, often in labs or field settings, focusing on data collection and analysis. Public Health Data Analysts typically work during daytime hours analyzing health data to inform policy and programs. While both roles require public health knowledge, they differ mainly in work hours, environment, and specific job functions.

What cities are hiring for Overnight Public Health Research jobs?

Cities with the most Overnight Public Health Research job openings:

What are the most commonly searched types of Public Health Research jobs?

The most popular types of Public Health Research jobs are:

What states have the most Overnight Public Health Research jobs?

States with the most job openings for Overnight Public Health Research jobs include:

Overnight Public Health Research jobs near you
Infographic showing various Overnight Public Health Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $96,670 per year, or $46.5 per hour.

Public Health Research Scientist

Mocksville, NC • On-site

22nd Century Limited, LLC
See more jobs at 22nd Century Limited, LLCexternal

Full-time

Posted 2 days ago

New

Job description

Public Health Research Scientist

Position Summary

The Public Health Research Scientist supports the planning, execution, and interpretation of public health research to advance the company's scientific and regulatory objectives. This position plays a key role in generating and evaluating evidence to support FDA applications such as the Premarket Tobacco Product Applications (PMTAs) and Supplemental PMTAs (SPMTAs), with a focus on demonstrating that products are appropriate for the protection of public health (APPH).

The successful candidate will collaborate with cross-functional teams to develop research strategies, oversee clinical and nonclinical studies, conduct scientific literature reviews, interpret research findings, and prepare high-quality scientific documentation. This role requires a strong foundation in public health research, human subjects research, and scientific communication.

Organizational Placement

The Public Health Research Scientist is a member of the Research and Development (R&D) department and reports directly to the Vice President of Science and Technology.

This position serves as the primary subject matter expert in public health research within the R&D team and works collaboratively with internal and external team members from Regulatory Affairs, Product Development, Analytical Chemistry, Quality, and CROs. The role provides scientific expertise that supports product development, evidence generation, and FDA regulatory submissions, while contributing to the company's overall research and innovation strategy.

As a member of a growing organization, the Public Health Research Scientist is expected to work collaboratively across functional areas, adapt to evolving business priorities, and contribute wherever scientific expertise is needed to support the company's mission and strategic objectives.


Essential Responsibilities

Public Health Research

  • Design, coordinate, and support public health research initiatives that inform regulatory and scientific decision-making.
  • Conduct systematic literature reviews and evidence syntheses to support research programs and regulatory submissions.
  • Evaluate epidemiologic, behavioral, clinical, and population health data to assess the potential public health impact of products.
  • Identify scientific evidence gaps and recommend research strategies to address them.

Clinical and Nonclinical Research Support

  • Assist in the planning, coordination, and execution of clinical and nonclinical research studies.
  • Develop and review study protocols, informed consent documents, case report forms, and study-related materials.
  • Collaborate with internal teams and external research partners to ensure studies are conducted according to approved protocols and applicable regulations.
  • Support the interpretation and integration of study findings into broader scientific evidence packages.

Human Subjects Research and Regulatory Compliance

  • Prepare and manage Institutional Review Board (IRB) submissions, amendments, continuing reviews, and study closeout documentation.
  • Ensure research activities comply with applicable ethical standards and regulations governing human subjects research.
  • Maintain documentation supporting research compliance and study oversight.

Regulatory and Scientific Support

  • Contribute scientific evidence to support PMTA and SPMTA submissions and other regulatory initiatives.
  • Prepare scientific summaries, technical reports, literature reviews, and regulatory documentation.
  • Assist in responding to regulatory information requests by compiling and interpreting scientific data.
  • Collaborate with Regulatory Affairs to ensure scientific documentation aligns with regulatory expectations.

Cross-Functional Collaboration

  • Coordinate activities with contract research organizations (CROs), academic collaborators, consultants, and external investigators.
  • Present research findings and scientific recommendations to technical teams and leadership.


Required Qualifications

  • Master's degree or Ph.D. in Public Health, Epidemiology, Health Sciences, Behavioral Science, Clinical Research, Biostatistics, or a related scientific discipline.
  • Minimum of three years of experience in public health research, clinical research, epidemiology, health outcomes research, or other evidence-based public health initiatives.
  • Experience designing, coordinating, or supporting clinical and/or nonclinical research studies.
  • Experience preparing and managing Institutional Review Board (IRB) submissions and ensuring compliance with applicable human subjects research requirements.
  • Strong understanding of research methodologies, study design, and scientific data analysis.
  • Experience conducting literature reviews, evidence synthesis, and interpreting scientific findings.
  • Excellent scientific writing skills with experience preparing technical reports, study summaries, manuscripts, or other scientific documentation.
  • Strong analytical, organizational, and project management skills.
  • Excellent written and verbal communication skills with the ability to communicate complex scientific concepts to multidisciplinary audiences.


Preferred Qualifications

  • Experience supporting FDA regulatory submissions, including PMTA, SPMTA, IND, NDA, 510(k), De Novo, IDE, or similar regulatory pathways.
  • Experience in tobacco regulatory science, pharmaceuticals, medical devices, consumer health products, or other regulated industries.
  • Knowledge of Appropriate for the Protection of Public Health (APPH) evaluations or population health assessment methodologies.
  • Experience with behavioral science, epidemiology, nicotine dependence research, abuse liability, consumer perception, or health outcomes research.
  • Experience collaborating with contract research organizations (CROs), academic institutions, or government agencies.


Knowledge, Skills, and Abilities

  • Strong understanding of public health research principles and evidence evaluation.
  • Ability to critically evaluate scientific literature and translate findings into actionable insights.
  • Knowledge of clinical research methods and ethical oversight of human subjects research.
  • Strong scientific writing, editing, and presentation skills.
  • Ability to manage multiple projects and competing priorities while maintaining attention to detail.
  • Strong interpersonal skills with the ability to build effective working relationships across scientific, clinical, and regulatory functions.
  • Commitment to scientific integrity, quality, and continuous learning.


Adaptability and Collaboration

 

  • As a growing organization, we value team members who are flexible, resourceful, and eager to contribute wherever needed. While this position has primary responsibilities in public health research, success in this role requires a willingness to wear multiple hats and support a variety of cross-functional initiatives.
  • The ideal candidate is comfortable working in a dynamic environment where priorities may shift. This may include assisting with regulatory strategy, scientific writing, project coordination, process improvement, or other activities that advance the company's mission and regulatory objectives.
  • We are looking for someone who is proactive, collaborative, and motivated to help build a high-performing organization by taking ownership, solving problems, and supporting teammates as needed.


Success Measures

Success in this role will be demonstrated by:

  • Delivery of high-quality scientific research and documentation that supports regulatory and business objectives.
  • Effective coordination and oversight of research activities and IRB processes.
  • Timely completion of assigned research projects and regulatory deliverables.
  • High-quality literature reviews and evidence syntheses that inform strategic decision-making.
  • Strong collaboration across cross-functional teams and external research partners.
  • Accurate, well-supported scientific analyses and technical reports.


Working Relationships

This position works closely with:

  • Regulatory Affairs
  • Clinical Affairs
  • Product Development
  • Toxicology
  • Analytical Chemistry
  • Biostatistics
  • Quality Assurance
  • External Contract Research Organizations (CROs)
  • Academic collaborators
  • Public health researchers and scientific consultants


Travel

Occasional travel (up to 15%) may be required for investigator meetings, scientific conferences, research site visits, or collaboration with external partners.

Apply