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Public Health Research Associate Jobs in Iowa (NOW HIRING)

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Public Health Research Associate information

What is a public health research associate?

Public Health Research Associates are professionals who support the design, implementation, and analysis of research projects aimed at improving public health outcomes. They typically collect and analyze data, assist with grant writing, and collaborate with other health professionals to address public health issues such as disease prevention, health education, and policy development. Their work helps inform evidence-based decisions and contributes to the advancement of public health practice and policy.

What are some common challenges faced by public health research associates when conducting fieldwork?

Public Health Research Associates often encounter challenges such as engaging hard-to-reach populations, ensuring data accuracy, and adhering to ethical guidelines during fieldwork. They may also face logistical issues like coordinating with community organizations, managing multiple projects, and working in diverse environments. Overcoming these challenges requires strong communication skills, cultural competence, and adaptability, as well as close collaboration with multidisciplinary teams and local stakeholders.

What are the key skills and qualifications needed to thrive as a public health research associate, and why are they important?

To thrive as a Public Health Research Associate, you need a strong background in epidemiology, statistics, and research methodology, typically supported by a degree in public health or a related field. Familiarity with statistical software like SPSS, SAS, or R and experience with data collection and analysis tools are commonly required. Strong written and verbal communication, attention to detail, and collaborative problem-solving skills help you excel in diverse research teams. These competencies ensure accurate data analysis, effective communication of findings, and the advancement of impactful public health initiatives.

What is the difference between Public Health Research Associate vs Epidemiologist?

AspectPublic Health Research AssociateEpidemiologist
Required CredentialsBachelor's or Master's in Public Health, Epidemiology, or related fieldMaster's or Doctorate in Epidemiology or Public Health
Work EnvironmentResearch settings, public health agencies, universitiesResearch institutions, government health departments, academia
Employer & Industry UsagePublic health organizations, NGOs, research firmsHealth departments, research institutes, academia
Common Search & ComparisonPublic Health Research Associate vs Epidemiologist

Public Health Research Associates typically hold bachelor's or master's degrees and work in research settings supporting public health projects. Epidemiologists usually have advanced degrees and focus on studying disease patterns and causes. Both roles are vital in public health but differ in scope, education, and responsibilities.

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

The most popular types of Public Health Research jobs in Iowa are:

What job categories do people searching Public Health Research Associate jobs in Iowa look for?

The top searched job categories for Public Health Research Associate jobs in Iowa are:

What cities in Iowa are hiring for Public Health Research Associate jobs?

Cities in Iowa with the most Public Health Research Associate job openings:

Infographic showing various Public Health Research Associate job openings in Iowa as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Senior Clinical Research Associate, Neuroscience (Contract)

11 Premier Research International LLC

Nevada, IA • On-site

$90 - $120/hr

Other

Posted 4 days ago


Job description

Premier Research is looking for a Senior Clinical Research Associate, Neuroscience (Contract) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. This is a full-time contract position for 6 months.

What You'll Be Doing:
  • Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan (CMP) timelines
  • Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and client requirements
  • Monitors (remote, on site or other approved mode of monitoring) with a focus on data integrity and subject safety in accordance with local/regional laws and country specific regulations
  • Plans day-to-day activities for monitoring of a clinical study and sets priorities per site
  • Prepares for and conducts on site and/or remote qualification, study initiation, interim monitoring, dosing observation, and close out monitoring visits as directed per CMP
  • Works with the Clinical Lead or equivalent to enhance and proactively manage site visits and trial issues during the monitoring phase
What We Are Searching For:
  • Must be located in CA, NV, GA, or FL
  • Neuroscience monitoring experience highly prioritized
  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
  • Patient facing, study coordinating experience preferred
  • Knowledge of ICH-GCP/ISO14155, FDA Guidance Documents, EU Directives, local/regional regulations, and drug/device development and clinical monitoring procedures
  • Knowledge of clinical/health systems as well as knowledge of cultural/professional practices appropriate to the country/region where site monitoring activities will be conducted
  • Ability to multitask and work effectively with technology and people in a fast-paced environment with changing priorities, self-starter
  • Travel up to 70-85%

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status

Premier Research is more than a company - it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems. Our Values - We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care - mirror the determination, flexibility and trust that our team embodies. As a Premier team member, you have the power to make an impact, regardless of job title and location. Our dedication to biotech and specialty pharma is unlike any other. We provide our staff with innovative technologies and continuous learning.

Introduce yourself to our Talent Team and we will reach out if there is a role that aligns with your experience and interests.

Premier Research is a global clinical research, product development, and consulting company. We are dedicated to helping biotech, specialty pharma, and MedTech innovators transform life-changing ideas and breakthrough science into new medical treatments. Our team is inspired by this common purpose. Premier is a place where you can change lives, and feel rewarded and celebrated. We aim high - we will not stop until we reach our goals. And we care about each other, about our customer and partners, and, most importantly, about all the patients that we touch with our work.

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