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Study Coordinator Jobs (NOW HIRING)

University of Utah

PS Study Coordinator

Campus, IL · On-site

The Study Coordinator will support our Clinical Research Coordinator in working on various research projects focused on skin cancer prevention, including a skin cancer preventive intervention in high ...

University of Utah

PS Study Coordinator

Campus, IL · On-site

The Study Coordinator will support our Clinical Research Coordinator in working on various research projects focused on skin cancer prevention, including a skin cancer preventive intervention in high ...

University of Utah

PS Study Coordinator

Campus, IL · On-site

The Study Coordinator will support our Clinical Research Coordinator in working on various research projects focused on skin cancer prevention, including a skin cancer preventive intervention in high ...

RPM ReSearch

Study Coordinator, Manager

Birmingham, AL · On-site

$80K - $110K/yr

Manager, Study Coordination & Quality Control Join a team driven by science, powered by people, and committed to improving lives. A GLP public CRO is seeking an experienced and passionate Manager ...

Neuralink

Preclinical Study Coordinator

Austin, TX

The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of ...

McKesson Corporation

Study Coordinator

Nashville, TN · On-site

As the Study Coordinator you will plan the execution and monitor the completion of complex Phase I-IV assigned clinical research protocols. Including abstracting, assembling and organizing research ...

University of Utah

Study Coordinators

Campus, IL · On-site

Responsibilities Study Coordinator Training and Assistance for Grantees Develop and deliver training materials and presentations to prepare grantees for evaluation activities. Attend grantee cohort ...

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$54.9K

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How much do study coordinator jobs pay per year?

As of Jun 6, 2026, the average yearly pay for study coordinator in the United States is $54,853.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $62,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What Is a Study Coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

What are study coordinators?

Study coordinators are professionals who manage the day-to-day operations of clinical research studies. They are responsible for tasks such as recruiting participants, ensuring protocol compliance, collecting and managing data, and maintaining communication between investigators, participants, and regulatory bodies. Study coordinators play a vital role in making sure that research studies are conducted ethically, efficiently, and according to regulatory guidelines. Their work ensures the integrity of study data and the safety of participants throughout the research process.

What are some common challenges Study Coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

More about Study Coordinator jobs
What cities are hiring for Study Coordinator jobs? Cities with the most Study Coordinator job openings:
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What states have the most Study Coordinator jobs? States with the most job openings for Study Coordinator jobs include:
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Study Coordinator jobs near you
Infographic showing various Study Coordinator job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 83% Full Time, 15% Part Time, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $54,853 per year, or $26.4 per hour.
Study Coordinator

Study Coordinator

Albert Einstein College of Medicine

Bronx, NY • On-site

$58K/yr

Full-time

Posted 16 days ago

Job description

The Study Coordinator will work on the asthma research team at Albert Einstein College of Medicine, the Children’s Hospital at Montefiore in the Bronx, NY.  The team’s research focuses on developing and evaluating interventions aimed at improving health outcomes for children with asthma.


We are seeking a highly organized and dedicated Study Coordinator to assist the Principal Investigator with coordinating ongoing and planned asthma-related projects. The Study Coordinator implements research project activities, ensuring the quality and integrity of data collection, and assists with the implementation of study protocols and materials. This job is fully in-person. This is an ideal position for someone able to commit a minimum of 2 years with plans to attend medical/graduate school. Individuals looking to establish a career in clinical research are also encouraged to apply.

The candidate will:

  • Oversee recruitment process.
  • Assist with study operations to ensure protocol compliance.
  • Serve as a liaison among study sites, participants, and stakeholders.
  • Organize and maintain documentation of participant and study data assuring accuracy.
  • Assist with preparing and submitting materials and progress reports for the Institutional Review Board (IRB), funding agencies and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion.
  • Manage participant tracking and maintain data integrity in study databases (e.g., REDCap, EHR exports) providing regular reports to the team leadership
  • Arrange meetings with study sites, medical directors and nursing staff, develop meeting agendas, PowerPoint presentations, and presents at meetings
  • Help train and support research staff and volunteers.
  • Assist in preparation of grant proposals, presentations, and dissemination activities.
  • Ensure adherence to the IRB-approved study protocol and procedures.
  • Performs other duties as assigned.

  • Bachelor’s Degree required.
  • ***Bilingual in English and Spanish required (able to read, write, speak as native speaker )***
  • Prior clinical research (minimum of 2 years) and asthma research experience is highly preferred
  • Life Sciences or Public Health background highly preferred
  • Research experience with children and families with asthma or chronic disease is highly preferred.
  • Strong computer skills: must be proficient in Microsoft Word, PowerPoint, and Excel. Redcap, and SPSS or other statistical software are a plus
  • Exceptional attention to detail and accuracy.
  • Excellent interpersonal, organizational, and communication skills
  • Time management and organization to conduct multiple studies.
  • Ability to manage multiple tasks and priorities while working as part of a team
  • Ability to work independently with minimal supervision, while adhering to study protocol.
  • Flexibility to work evenings and weekends.

USD $58,500.00/Yr.

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