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Community Research Coordinator Jobs (NOW HIRING)

... community-based healthcare and through our services that unburden the patients and principal ... We seek a Research Coordinator (Independent Contractor) to join our team in St. Louis, MO! As an ...

The Clinical Research Coordinator (CRC) is a specialized research professional working with and ... Our success is anchored in our trusted digital platforms that engage physician communities globally ...

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Community Research Coordinator information

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$21.5K

$80.6K

$112.5K

How much do community research coordinator jobs pay per year?

As of May 28, 2026, the average yearly pay for community research coordinator in the United States is $80,570.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $99,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Community Research Coordinator, and why are they important?

To thrive as a Community Research Coordinator, you need a solid background in research methods, data collection, and community engagement, usually supported by a bachelor's or master's degree in social sciences or public health. Familiarity with survey software, database management systems, and data analysis tools like SPSS or Excel is typically required. Strong interpersonal skills, cultural sensitivity, and effective communication distinguish top performers in this role. These skills ensure accurate data gathering, foster trust within communities, and drive successful research outcomes.

What are some common challenges faced by Community Research Coordinators in managing multiple projects simultaneously?

Community Research Coordinators often juggle several projects at once, each with unique timelines, stakeholder needs, and data collection requirements. Balancing these demands can be challenging, especially when coordinating with community partners, managing participant recruitment, and ensuring data quality and compliance with ethical standards. Strong organizational skills, clear communication, and the ability to prioritize tasks are essential to navigate these complexities. Collaborating closely with research teams and community members helps ensure that all projects progress smoothly and that any issues are addressed promptly.

What does a Community Research Coordinator do?

A Community Research Coordinator manages and implements research projects that involve community participation. They serve as a liaison between research teams and community members, ensuring that studies are culturally sensitive and ethically conducted. Their responsibilities include recruiting participants, collecting and managing data, organizing community meetings, and communicating research findings. This role is vital in building trust with communities and ensuring research reflects their needs and perspectives.

What is the salary difference between CRA and CRC?

Community Research Coordinators (CRCs) typically earn a lower salary than Clinical Research Associates (CRAs), with CRAs often earning 10-20% more due to their additional responsibilities and required certifications. Salaries for both roles vary based on experience, location, and organization, but CRAs generally have higher compensation due to their oversight and monitoring duties in clinical trials.
More about Community Research Coordinator jobs
What cities are hiring for Community Research Coordinator jobs? Cities with the most Community Research Coordinator job openings:
What are the most commonly searched types of Community Research jobs? The most popular types of Community Research jobs are:
What states have the most Community Research Coordinator jobs? States with the most job openings for Community Research Coordinator jobs include:
Infographic showing various Community Research Coordinator job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $80,570 per year, or $38.7 per hour.
Clinical Research Coordinator or Research Assistant

Clinical Research Coordinator or Research Assistant

Avera

Pierre, SD โ€ข On-site

$20.75 - $36.50/hr

Full-time, Part-time

Retirement, PTO

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Location:

Avera St Mary's Hospital

Worker Type:

Regular

Work Shift:

Day Shift (United States of America)

Pay Range:

The pay range for this position is listed below. Actual pay rate dependent upon experience.

$20.75 - $36.50

Position Highlights

This position requires relocation to Pierre, South Dakota.

We are looking for either a Clinical Research Coordinator or Research Assistant This can be a Full Time or Part time Position.

This position will support projects in the maternal and child health studies at Avera Research Institute. This includes supporting the ECHO study (Environmental influences on Child Health Outcomes), which is a longitudinal, observational study following pregnant women and their children to understand how environmental exposures in the prenatal and early childhood time frame affect health outcomes for children later in life.

To learn more about some of the main projects, including the ECHO program, please click here : https://echochildren.org/

The requirements for this position are listed below.

Research Assistant: High School Diploma or GED

Clinical Research Coordinator: Bachelors from a four year college or university within the health and science field.

The pay range for this position is listed below. Actual pay rate dependent upon experience.

Research Assistant: $20.50 - $27.00

Clinical Research Coordinator: $24.00 - $36.50

Clinical Research Coordinator Brief Overview

An advanced position that contributes to the overall operations of one or more research studies. The CRC is responsible for implementation of the study protocol, recruitment plan, study visits, data, study assessments, and other tasks outlined in the protocol. This position requires close collaboration with the study team and investigator to ensure safe and compliant research procedures and follow-up per the established research protocol. This position will work directly with research participants, physicians, nurses, community stakeholders, and health/social service organizations. This position has opportunities for ongoing learning and contribution to research that is focused on improving health and wellbeing of individuals and the community.

Research Assistant Brief Overview

Works under general direction to perform professional level medical or scientific research assignments. Performs diverse and complex duties, with a focus on entering patient data into a variety of computer based systems, scheduling of daily activities, tracking specimens, retention and organization of documentation, and data functions for staff.

You Belong at Avera

Be part of a multidisciplinary team built with compassion and the goal of Moving Health Forward for you and our patients. Work where you matter.

A Brief Overview

An advanced position that contributes to the overall operations of one or more research studies. The CRC is responsible for implementation of the study protocol, recruitment plan, study visits, data, study assessments, and other tasks outlined in the protocol. This position requires close collaboration with the study team and investigator to ensure safe and compliant research procedures and follow-up per the established research protocol. This position will work directly with research participants, physicians, nurses, community stakeholders, and health/social service organizations. This position has opportunities for ongoing learning and contribution to research that is focused on improving health and wellbeing of individuals and the community.

What you will do

  • Coordinates research studies per Good Clinical Practices guidelines, FDA regulations, and approved protocols.
  • Understands and adheres to Standard Operating Procedures (SOPs). Ability to develop or improve SOPs, help guides, and other team resources.
  • Acquires detailed knowledge of assigned research protocols and ability to conduct study required processes, procedures, and assessments. Ability to prepare, utilize, and review Case Report Forms. Collects and manages data, Case Report Forms, and timely entry into the electronic data capture system.
  • Collects and assists with processing all laboratory specimens to include centrifuging, separating, measuring, storing, shipping, and distributing to appropriate testing areas. Maintains inventory of laboratory supplies and study kits.
  • Screens, recruits, and enrolls study participants using study's eligibility criteria. Preforms the informed consent, answering all participant questions, and obtaining appropriate sign-off.
  • Ensures the adherence to ethical practices during the conduct of clinical trials in order to protect the rights and well-being of patients and the collection of quality data.
  • Ensures validity of research results by ensuring timely, accurate, and complete data documentation, reporting deviations, violations, and serious adverse events.
  • Develops relationships with referring physicians, clinical staff, and ancillary departments to facilitate compliance with and accrual to clinical trials.

Essential Qualifications

The individual must be able to work the hours specified. To perform this job successfully, an individual must be able to perform each essential job function satisfactorily including having visual acuity adequate to perform position duties and the ability to communicate effectively with others, hear, understand and distinguish speech and other sounds. These requirements and those listed above are representative of the knowledge, skills, and abilities required to perform the essential job functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions, as long as the accommodations do not cause undue hardship to the employer.

Required Education, License/Certification, or Work Experience:

  • Bachelor's From a four year college or university within the health and science field

Preferred Education, License/Certification, or Work Experience:

  • 1-3 years Human Research
  • 1-3 years Laboratory or clinical

Expectations and Standards

  • Commitment to the daily application of Avera's mission, vision, core values, and social principles to serve patients, their families, and our community.
  • Promote Avera's values of compassion, hospitality, and stewardship.
  • Uphold Avera's standards of Communication, Attitude, Responsiveness, and Engagement (CARE) with enthusiasm and sincerity.
  • Maintain confidentiality.
  • Work effectively in a team environment, coordinating work flow with other team members and ensuring a productive and efficient environment.
  • Comply with safety principles, laws, regulations, and standards associated with, but not limited to, CMS, The Joint Commission, DHHS, and OSHA if applicable.

Benefits You Need & Then Some

Avera is proud to offer a wide range of benefits to qualifying part-time and full-time employees. We support you with opportunities to help live balanced, healthy lives. Benefits are designed to meet needs of today and into the future.

  • PTO available day 1 for eligible hires.
  • Up to 5% employer matching contribution for retirement
  • Career development guided by hands-on training and mentorship

Avera is an Equal Opportunity Employer - Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, Veteran Status, or other categories protected by law. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-605-504-4444 or send an email to talent@avera.org .

At Avera, the way you are treated as an employee translates into the compassionate care you deliver to patients and team members. Because we consider health care a ministry, you can live out your faith, uphold the dignity and respect of all persons while not compromising high-quality services. Join us in making a positive impact on moving health forward.

The policy of Avera to provide opportunities for all qualified employees or applicants without regard to disability and to provide reasonable accommodations for all employees or applicants who may be disabled. Avera is committed to ensuring compliance in accordance with the Americans with Disability Act. For assistance, please contact HR Now at 605-504-4444.

Additional Notices:

For TTY, dial 711

Avera is an Equal Opportunity/Affirmative Action Employer: Minority/Female/Disabled/Veteran/Sexual Orientation/Gender Identity.


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About Avera

Sourced by ZipRecruiter

Avera is a fully integrated, partnership-driven development, construction, and investment firm that is dedicated to providing the highest quality real estate assets for our clients and partners through innovation, value creation and integrity. Avera is one of the most active firms in the United States, leading the industry in office and industrial development. We are experts in on-time project delivery, construction and development efficiencies, and budget practices. Utilizing these processes allows us to exceed customer satisfaction and project objectives, while maintaining the highest level of quality in every project.

Industry

Real estate

Company size

11 - 50 Employees

Headquarters location

Houston, TX, US

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