Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies * Familiarity with the Microsoft Office Suite * Previous work with CRFs and EDC * Excellent organizational skills to independently ...
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies * Familiarity with the Microsoft Office Suite * Previous work with CRFs and EDC * Excellent organizational skills to independently ...
... OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). * Must be knowledgeable in internet access to manage clinical trials ...
... OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). * Must be knowledgeable in internet access to manage clinical trials ...
RN
Whittier, CA · On-site
... OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). * Must be knowledgeable in internet access to manage clinical trials ...
RN
Whittier, CA · On-site
... OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). * Must be knowledgeable in internet access to manage clinical trials ...
Senior Biorepository Data Analyst
$81K - $102K/yr
Demonstrates an understanding of and proficiency with the application of all compliance and reporting requirements respective HIPAA and OHRP. * Advises and guides PIs and other investigators on data ...
Senior Biorepository Data Analyst
$81K - $102K/yr
Demonstrates an understanding of and proficiency with the application of all compliance and reporting requirements respective HIPAA and OHRP. * Advises and guides PIs and other investigators on data ...
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coord
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coord
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coord
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coord
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coord
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coord
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coordinator-GU
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Clinical Study Coordinator-GU
Duarte, CA · On-site
Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies * Familiarity with the Microsoft Office Suite * Previous work with CRFs and EDC * Excellent organizational skills to independently ...
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies * Familiarity with the Microsoft Office Suite * Previous work with CRFs and EDC * Excellent organizational skills to independently ...
Cardiovascular Clinical Research Nurse
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Cardiovascular Clinical Research Nurse
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinician Research Nurse
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinician Research Nurse
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinician Research Nurse
Chandler, AZ · On-site
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinician Research Nurse
Chandler, AZ · On-site
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinician Research Nurse
Chandler, AZ · On-site
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinician Research Nurse
Chandler, AZ · On-site
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinical Research RN
Phoenix, AZ · On-site
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Clinical Research RN
Phoenix, AZ · On-site
$32.38 - $48.17/hr
Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) * Complies with licensure, contractual, protocol and policy requirements
Expert knowledge of clinical research regulations and oversight frameworks (FDA, ICH‑GCP, OHRP, NIH, HIPAA, IRB). * Proven ability to design and scale clinical research infrastructure, SOPs ...
Quick apply
Expert knowledge of clinical research regulations and oversight frameworks (FDA, ICH‑GCP, OHRP, NIH, HIPAA, IRB). * Proven ability to design and scale clinical research infrastructure, SOPs ...
Ohrp information
See salary details
$50K - $62.8K
1% of jobs
$62.8K - $75.5K
4% of jobs
$75.5K - $88.3K
6% of jobs
$88.3K - $101.1K
10% of jobs
$105.7K is the 25th percentile. Wages below this are outliers.
$101.1K - $113.9K
10% of jobs
$113.9K - $126.6K
17% of jobs
The median wage is $127.9K / yr.
$126.6K - $139.4K
16% of jobs
$149K is the 75th percentile. Wages above this are outliers.
$139.4K - $152.2K
14% of jobs
$152.2K - $165K
10% of jobs
$165K - $177.7K
6% of jobs
$177.7K - $190.5K
5% of jobs
$50K
$130.8K
$190.5K
How much do ohrp jobs pay per year?
As of Jun 8, 2026, the average yearly pay for ohrp in the United States is $130,847.00, according to ZipRecruiter salary data. Most workers in this role earn between $105,500.00 and $153,000.00 per year, depending on experience, location, and employer.
What are the main responsibilities of someone working in an OHRP (Office for Human Research Protections) compliance role?
An OHRP compliance professional is primarily responsible for ensuring that research involving human subjects adheres to federal regulations, ethical guidelines, and institutional policies. This often involves reviewing research protocols, providing guidance to investigators, conducting compliance audits, and offering training on human subject protections. Collaboration with researchers, Institutional Review Boards (IRBs), and administrative staff is central to the role, as is staying updated on evolving regulatory requirements. The work environment is typically detail-oriented and requires strong communication skills to address and resolve complex ethical issues.
What are OHRP professionals?
OHRP stands for the Office for Human Research Protections. Professionals working at or with OHRP are responsible for ensuring the protection of the rights, welfare, and well-being of human subjects involved in research conducted or supported by the U.S. Department of Health and Human Services (HHS). They provide leadership in the field of human subjects protections, develop policy guidance, offer educational resources, and oversee compliance with regulations such as the Common Rule. OHRP professionals may include compliance specialists, policy analysts, and educators who work collaboratively with research institutions and investigators.
What are the key skills and qualifications needed to thrive as an OHRP (Office for Human Research Protections) professional, and why are they important?
To thrive as an OHRP professional, you need a solid background in research ethics, regulatory compliance, and human subject protections, often supported by an advanced degree in health, law, or a related field. Familiarity with federal regulations like the Common Rule, IRB management systems, and compliance tracking tools is essential. Strong analytical thinking, attention to detail, and effective communication are valuable soft skills in this role. These competencies are crucial to ensure ethical research practices and protect the rights and welfare of research participants.
What is the difference between Ohrp vs Clinical Research Coordinator?
| Aspect | Ohrp | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Typically requires knowledge of human research protections, IRB regulations, and sometimes certifications like CITI | Often requires knowledge of study protocols, patient interaction, and sometimes certifications like CITI |
| Work Environment | Research institutions, hospitals, or universities overseeing human subject research | Hospitals, clinics, or research sites managing patient studies |
| Employer & Industry Usage | Used mainly in research oversight and compliance roles | Commonly employed in clinical settings managing patient studies |
| Common Search & Comparison Intent | Understanding regulatory roles and compliance | Managing clinical trials and patient data |
The main difference between Ohrp and Clinical Research Coordinator lies in their focus: Ohrp primarily oversees research compliance and human subject protections, while Clinical Research Coordinators handle the day-to-day management of clinical trials and patient interactions. Both roles are essential in clinical research but serve different functions within the research process.
City Of Hope rating
8.4
Based on 87 frontline employees who took The Breakroom Quiz
33rd of 869 rated healthcare providers
Job description
Clinical Study Coordinator - Clinical Research (On-Site)-Duarte
Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today.
Orange County Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials. Under the supervision of the Director, Clinical Research, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations, strong organizational skills, and the ability to collaborate with investigators and clinical staff in a fast-paced environment.
As a successful candidate, you will:
- Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.
- Follow and execute clinical trial protocols and procedures.
- Coordinate participant recruitment, informed consent, and care.
- Communicate with participants, investigators, and sponsors to ensure clear understanding and compliance.
- Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.
- Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and maintain necessary certifications and licensure.
Qualifications - External
Qualifications - External
Qualifications - External
Your qualifications should include:
- Bachelor's degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education.
- Minimum of 2 years research or relevant clinical experience
- ACRP or SOCRA certification within 1 year of employment
- International Air Transport Association (IATA) within 1 month of employment
- Good Clinical Practice (GCP) within 1 month of employment
- Human Subjects Protection (HSP) within 1 month of employment
- Basic Life Support (BLS) within 1 month of employment
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.
City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here.
To learn more about our Comprehensive Benefits, please CLICK HERE.
What City Of Hope employees say
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About City of Hope
Sourced by ZipRecruiter
City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hopes translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hopes specialized cancer expertise. City of Hope is ranked among the nations Best Hospitals in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.
Industry
Hospitals
Company size
1,001 - 5,000 Employees
Headquarters location
Duarte, CA, US
Year founded
1913