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Research Ethics Jobs (NOW HIRING)

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal ...

Mercyagedcare

Research Manager

Anoka, MN · Hybrid

Support researchers with ethics and governance processes, study conduct, funding opportunities and translating research into practice. * Work with clinical services, internal teams, universities ...

ATSU PUBLIC

ASDOH - Student Research Assistant

Mesa, AZ · On-site

$13.50 - $17/hr

This position also supports professional development in research ethics, data management, and clinical research operations. Duties & Responsibilities: * Recruit participants to the project. * Obtain ...

Howard University

Research Assistant

Washington, DC · On-site

$20/hr

Demonstrates understanding of research ethics and confidentiality MINIMUM REQUIREMENTS: * Currently enrolled as an undergraduate student (freshman-senior level) in a relevant field (e.g., Biology ...

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How much do research ethics jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for research ethics 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 is research ethics?

A Research Ethics job involves ensuring that research involving human participants, animals, or sensitive data is conducted ethically and in compliance with regulations. Professionals in this field review study protocols, provide ethical guidance, and ensure adherence to institutional, national, and international ethical standards. They may work on issues like informed consent, privacy protection, and minimizing harm to participants. Their role is crucial in maintaining the integrity and ethical responsibility of research practices.

What does someone working in research ethics do?

Professionals in Research Ethics regularly review research proposals for ethical compliance, advise researchers on best practices, and ensure adherence to federal and institutional regulations. They may coordinate and facilitate Institutional Review Board (IRB) meetings, conduct educational sessions for research staff, and handle the review of adverse event reports. Frequent collaboration with researchers, administrators, and legal teams is common to ensure all ethical issues are addressed proactively. The nature of the work often involves balancing regulatory requirements with the advancement of innovative research.

What are the key skills and qualifications needed to thrive in research ethics?

To thrive in Research Ethics, a strong background in bioethics, research compliance, and regulatory guidelines is essential, often supported by an advanced degree in a relevant field and experience with IRB protocols. Familiarity with electronic submission systems for ethical review and certifications such as Certified IRB Professional (CIP) are commonly needed. Excellent critical thinking, clear communication, and the ability to facilitate collaborative discussions set exceptional candidates apart. These skills ensure ethical research practices, safeguard participants’ rights, and maintain institutional and regulatory standards.

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Research Ethics jobs near you
Infographic showing various Research Ethics job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $46,222 per year, or $22.2 per hour.

Clinical Research Coordinator

Winaxis

Dallas, TX • On-site

$24 - $32/hr

Full-time

Re-posted 22 days ago

Job description

Job Summary: The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical trials in accordance with study protocols, Good Clinical Practice (GCP) guidelines, institutional policies, and applicable regulatory requirements. The role involves participant recruitment, study documentation, data collection, and ensuring the smooth execution of research activities while safeguarding participant safety and data integrity. Key Responsibilities: Coordinate and oversee day-to-day activities related to assigned clinical studies. Review study protocols and ensure all trial activities are conducted in compliance with protocol requirements. Recruit, screen, and enroll eligible study participants according to inclusion and exclusion criteria. Obtain and document informed consent from study participants prior to study procedures. Schedule participant visits and coordinate study assessments, procedures, and follow-ups. Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study records. Monitor participant safety by identifying, documenting, and reporting adverse events and serious adverse events in accordance with regulatory timelines. Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs), laboratory personnel, and other study stakeholders. Prepare for and support sponsor monitoring visits, audits, and regulatory inspections. Ensure adherence to Good Clinical Practice (GCP), institutional policies, and applicable local and international regulations. Track study timelines, recruitment targets, and protocol milestones. Assist with study initiation, amendments, close-out activities, and archiving of study documents. Maintain confidentiality of participant information and research data at all times. Required Qualifications: Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related healthcare field. Prior experience in clinical research or clinical trial coordination is preferred. Certification in Good Clinical Practice (GCP) is an advantage. Required Skills: Strong understanding of clinical trial processes and research ethics. Knowledge of ICH-GCP guidelines and regulatory requirements. Excellent organizational and time-management skills. Strong verbal and written communication abilities. Attention to detail and accuracy in documentation. Proficiency in Microsoft Office applications and EDC systems. Ability to work independently and collaboratively within multidisciplinary teams. Effective problem-solving and interpersonal skills. Working Conditions: Work is typically performed in hospitals, research institutions, academic medical centers, or clinical research organizations. May require flexibility to accommodate participant schedules and sponsor visits.