CITI Human Subjects Protection Training and/or Good Clinical Practice (GCP) certification preferred ... Strong analytical and quantitative abilities. * Excellent written and verbal communication skills.
CITI Human Subjects Protection Training and/or Good Clinical Practice (GCP) certification preferred ... Strong analytical and quantitative abilities. * Excellent written and verbal communication skills.
... analysis of clinical research data. A CRN may work independently or as a member of a team. They ... Understand and adhere to all IRB requirements, Human Subjects protection regulations, and all ...
... analysis of clinical research data. A CRN may work independently or as a member of a team. They ... Understand and adhere to all IRB requirements, Human Subjects protection regulations, and all ...
... GCP), Human Subjects Protection, and applicable regulatory guidelines. * Develop and maintain ... Generate reports and organize data for statistical analysis. * Assist with the preparation and ...
... GCP), Human Subjects Protection, and applicable regulatory guidelines. * Develop and maintain ... Generate reports and organize data for statistical analysis. * Assist with the preparation and ...
IRB Operations Manager
Princeton, NJ · On-site
Provide regulatory guidance to investigators and research teams on human subjects protection ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...
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IRB Operations Manager
Princeton, NJ · On-site
Provide regulatory guidance to investigators and research teams on human subjects protection ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...
IRB Operations Manager
Princeton, NJ · On-site
$130K - $170K/yr
Provide regulatory guidance to investigators and research teams on human subjects protection ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...
IRB Operations Manager
Princeton, NJ · On-site
$130K - $170K/yr
Provide regulatory guidance to investigators and research teams on human subjects protection ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...
Research Nurse
$45 - $50/hr
Ensure informed consent process and human subjects protection in clinical research and counsel ... Excellent analytical, organizational and time management skills. The total hourly pay for this ...
Research Nurse
$45 - $50/hr
Ensure informed consent process and human subjects protection in clinical research and counsel ... Excellent analytical, organizational and time management skills. The total hourly pay for this ...
IRB Operations Manager
Princeton, NJ · On-site
Provide regulatory guidance to investigators and research teams on human subjects protection ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...
IRB Operations Manager
Princeton, NJ · On-site
Provide regulatory guidance to investigators and research teams on human subjects protection ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...
... GCP), Human Subjects Protection, and applicable regulatory guidelines. * Develop and maintain ... Generate reports and organize data for statistical analysis. * Assist with the preparation and ...
... GCP), Human Subjects Protection, and applicable regulatory guidelines. * Develop and maintain ... Generate reports and organize data for statistical analysis. * Assist with the preparation and ...
... GCP), Human Subjects Protection, and applicable regulatory guidelines. * Develop and maintain ... Generate reports and organize data for statistical analysis. * Assist with the preparation and ...
... GCP), Human Subjects Protection, and applicable regulatory guidelines. * Develop and maintain ... Generate reports and organize data for statistical analysis. * Assist with the preparation and ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Periodically reviews Command Assurances for the protection of human research subjects. Assurance ... Performs full range of subject matter research and analyses. * Interprets results to determine ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Periodically reviews Command Assurances for the protection of human research subjects. Assurance ... Performs full range of subject matter research and analyses. * Interprets results to determine ...
Overview The Clinical Research Nurse I performs a variety of clinical and non-clinical tasks ... Adhere to and maintain Good Clinical Practice (GCP)/Human Subjects Protection (HSP) practices and ...
Overview The Clinical Research Nurse I performs a variety of clinical and non-clinical tasks ... Adhere to and maintain Good Clinical Practice (GCP)/Human Subjects Protection (HSP) practices and ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Periodically reviews Command Assurances for the protection of human research subjects. Assurance ... Performs full range of subject matter research and analyses. * Interprets results to determine ...
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
Periodically reviews Command Assurances for the protection of human research subjects. Assurance ... Performs full range of subject matter research and analyses. * Interprets results to determine ...
Clinical Research Nurse I The Clinical Research Nurse I performs a variety of clinical and non ... Adhere to and maintain Good Clinical Practice (GCP)/Human Subjects Protection (HSP) practices and ...
Clinical Research Nurse I The Clinical Research Nurse I performs a variety of clinical and non ... Adhere to and maintain Good Clinical Practice (GCP)/Human Subjects Protection (HSP) practices and ...
Human Subjects Research Coordinator- II
Rochester, NY · On-site
$25.14 - $35.24/hr
Word processing and data analysis software required* Knowledge of Microsoft Office and Windows ... law (Protected Characteristics). This commitment extends to non-discrimination in the ...
Human Subjects Research Coordinator- II
Rochester, NY · On-site
$25.14 - $35.24/hr
Word processing and data analysis software required* Knowledge of Microsoft Office and Windows ... law (Protected Characteristics). This commitment extends to non-discrimination in the ...
Generate reports and organize data for statistical analysis.* Assist with the preparation and ... Working knowledge of Good Clinical Practice (GCP), Human Subjects Protection, IRB processes, and ...
Generate reports and organize data for statistical analysis.* Assist with the preparation and ... Working knowledge of Good Clinical Practice (GCP), Human Subjects Protection, IRB processes, and ...
Clinical Research Nurse Coordinator
Little Rock, AR · On-site
$66K - $83K/yr
The Clinical Research Nurse upholds standards for human subjects protection. Additional Information ... Analyst "We are an organization of care, love, and hope while we champion children." Angela ...
Clinical Research Nurse Coordinator
Little Rock, AR · On-site
$66K - $83K/yr
The Clinical Research Nurse upholds standards for human subjects protection. Additional Information ... Analyst "We are an organization of care, love, and hope while we champion children." Angela ...
Human Subjects Research Coordinator II
$25.14 - $35.24/hr
Word processing and data analysis software required * Experience as Human Subject Research ... law (Protected Characteristics). This commitment extends to non-discrimination in the ...
Human Subjects Research Coordinator II
$25.14 - $35.24/hr
Word processing and data analysis software required * Experience as Human Subject Research ... law (Protected Characteristics). This commitment extends to non-discrimination in the ...
Human Subjects Research Coordinator II
Rochester, NY · On-site
$25.14 - $35.24/hr
Word processing and data analysis software required * Experience as Human Subject Research ... law (Protected Characteristics). This commitment extends to non-discrimination in the ...
Human Subjects Research Coordinator II
Rochester, NY · On-site
$25.14 - $35.24/hr
Word processing and data analysis software required * Experience as Human Subject Research ... law (Protected Characteristics). This commitment extends to non-discrimination in the ...
IRB Compliance Analyst
Fort Worth, TX · On-site
... Protection Program (HRPP) and Institutional Review Board (IRB). The position assists with intake ... human subjects research submissions in Cayuse Human Ethics, including initial studies ...
IRB Compliance Analyst
Fort Worth, TX · On-site
... Protection Program (HRPP) and Institutional Review Board (IRB). The position assists with intake ... human subjects research submissions in Cayuse Human Ethics, including initial studies ...
Completion of CITI Human Subjects Protection and Good Clinical Practice Certifications upon hiring ... research, patient privacy, electronic medical record use, HIPPA, and the UCSF code of conduct.
Completion of CITI Human Subjects Protection and Good Clinical Practice Certifications upon hiring ... research, patient privacy, electronic medical record use, HIPPA, and the UCSF code of conduct.
Human Subjects Protection Research Analyst information
See salary details
$38.5K - $44K
1% of jobs
$44K - $49.6K
3% of jobs
$49.6K - $55.1K
3% of jobs
$57.3K is the 25th percentile. Wages below this are outliers.
$55.1K - $60.7K
45% of jobs
$60.7K - $66.2K
5% of jobs
$66.2K - $71.8K
4% of jobs
$71.8K - $77.3K
3% of jobs
$77.3K - $82.9K
3% of jobs
$82.9K - $88.4K
2% of jobs
$88.4K - $94K
2% of jobs
$94.4K is the 75th percentile. Wages above this are outliers.
$94K - $99.5K
27% of jobs
$38.5K
$74K
$99.5K
How much do human subjects protection research analyst jobs pay per year?
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Research Specialist
Valhalla, NY
$90K/yr
Full-time
Posted 5 days ago
Touro University rating
5.9
Based on 13 frontline employees who took The Breakroom Quiz
Job description
The Research Specialist - Epidemiology will support clinical, translational, outcomes, and population health research activities within the Department of Medicine. The incumbent will participate in the design, implementation, coordination, analysis, and dissemination of research studies focused on clinical outcomes, epidemiology, quality improvement, and health services research. Responsibilities include management of research databases, regulatory compliance, protocol development, statistical support, participant recruitment, data collection, and preparation of scientific reports, abstracts, publications, and grant-related materials. The position requires close collaboration with faculty investigators, research staff, institutional offices, and external research partners to advance the Department's research mission.
Responsibilities- Coordinate and manage clinical and epidemiologic research studies, including protocol implementation, participant recruitment, data collection, database maintenance, and study documentation.
- Assist faculty investigators with research protocol development, literature reviews, study design, statistical analyses, interpretation of findings, and preparation of scientific manuscripts and presentations.
- Prepare and maintain regulatory documents, IRB submissions, informed consent materials, and study records in compliance with federal regulations, institutional policies, and Good Clinical Practice guidelines.
- Develop, maintain, analyze, and validate research databases using statistical and data management software; generate reports and summaries to support ongoing research initiatives.
- Collaborate effectively with investigators, research coordinators, study sponsors, institutional offices, and external collaborators while maintaining high standards of communication, organization, compliance, and teamwork
- Master's Degree in Epidemiology, Public Health, Clinical Research, Health Sciences, Biostatistics, Medicine, or a related scientific discipline required. Doctoral degree preferred.
- CITI Human Subjects Protection Training and/or Good Clinical Practice (GCP) certification preferred.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook); experience with REDCap, statistical analysis software (SAS, SPSS, Stata, or R), data management tools, and electronic medical record systems preferred.
- Minimum three years of experience in clinical research, epidemiologic research, outcomes research, public health, or a related research environment.
- Experience with human subjects research and regulatory compliance preferred.
- Strong analytical and quantitative abilities.
- Excellent written and verbal communication skills.
- Strong organizational and project management skills.
- Ability to work independently and as part of a multidisciplinary team.
- Demonstrated attention to detail and commitment to data quality.
- Experience preparing manuscripts, abstracts, grant applications, and scientific reports preferred.
- Routine use of computers and office equipment. Ability to sit for extended periods and occasionally travel between NYMC, Westchester Medical Center, and affiliated research sites.
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