Clinical Research Coordinator II - Part Time

Shriners Children's; Sacramento (CA); On-site; USD 92,839,000 - 139,259,000; Full time

Job summary

Shriners Children’s is seeking a Clinical Research Coordinator, Level 2 (CRC2) to oversee and ensure compliant clinical research activities across SHC. You will support protocol development, recruitment, consent, data collection, and safeguarding of pediatric subjects.

Reporting to the Clinical Research Program Manager, you will work with SHC staff and sponsors to maintain data quality, regulatory adherence, and patient safety, upholding Belmont Report and ICH-GCP standards.

Qualifications

• 5+ years of experience in clinical research administration.
• 3+ years of clinical research experience including site/study management, IRBs, and federal regulations.
• Knowledge of electronic health systems and databases used in research.
• Familiarity with regulations related to clinical research and informed consent.
• Knowledge of Belmont Report, Nuremberg Code and ICH-GCP standards.
• Experience with large-scale data collection initiatives.
• Awareness of sponsor policies and procedures.

Responsibilities

• Maintain knowledge of regulatory requirements in clinical research.
• Track study, investigator and IRB information and patient recruitment activity.
• Coordinate data collection, statistical analysis and dissemination of results.
• Prepare study results for dissemination to research teams.
• Uphold patient safety and data privacy throughout the study.
• Collaborate with SHC leadership to ensure research mission is upheld.
• Maintain scientific integrity and excellence.

Skills

Clinical research

Regulatory compliance

Data integrity

IRB knowledge

Ethical standards

Belmont Report

Education

Bachelor's degree

CCRP or CCRC certification

Job description

Company OverviewShriners Children’s is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family’s ability to pay or insurance status. Please click here to learn more about our locations.CURRENT EMPLOYEES: Please log into Workday Click Here to apply internally through the \"Jobs Hub\"Job DescriptionThe Clinical Research Coordinator, Level 2 (CRC2) is a specialized, independent research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities. Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and Research Programs Office at SHC International Headquarters, the CRC provides support in accordance with SHC's policies and procedures, hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. The CRC works closely with the Chief of Staff, SHC scientific and medical staff and other research personnel to ethically recruit and consent SHC's vulnerable pediatric subjects and to appropriately collect and safeguard data. Overall, the CRC is the site's primary liaison among research participants, the local investigator(s) and study sponsor(s). This position's main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.Key Responsibilities:Maintains a contemporary knowledge of clinical research regulatory requirements. Has a working knowledge of the complex clinical research process, from protocol development to implementationResponsible for tracking all aspects of projects including all study, investigator and Institutional Review Board (IRB) information, patient recruitment activity, and financial managementCoordinates the collection, statistical analysis and dissemination of data results throughout a clinical studyContributes in compiling, critically analyzing and preparing study results to share with research teamDemonstrates knowledge of ethical standards set forth by the Belmont Report, the Nuremberg Code and the International Conference of Harmonization GCP standardsMaintains patient safety and privacy throughout the studyWorks effectively with SHC leadership to ensure the research mission is upheldMaintains scientific integrity, intellectual honesty, and excellenceRequired Qualifications:Without a Bachelor's degree, 5 or more years of specific job-related experience in the administration of clinical research is required3 or more years of clinical research experience, e.g. experience with site management, study management, IRB's, and federal regulations regarding clinical research complianceKnowledge of, or ability to learn, electronic health system and databases used in research environmentsWorking knowledge of regulation and guidance(s) related to clinical researchKnowledge of, or ability to learn, participant and sample collection for large scale initiativesWorking knowledge of the applicable regulations related to product or agent being studied, the specific protocol, the informed consent process, and the sponsors' policies and proceduresPreferred Qualifications:Bachelor's or Master's Clinical Research, science or other health-care related fieldCCRP or CCRC certificationExperience in the coordination of intergroup or multi-site clinical studiesThe pay range for this position is $32.40 - $48.60/hour.Compensation is determined based on years of relevant experience and departmental equity.