Clinical Research Coordinator II - Part Time

Shriners Children's; Sacramento (CA); On-site; USD 45,000 - 67,000; Full time

Job summary

Shriners Children’s in California seeks a Clinical Research Coordinator, Level 2 (CRC2) to oversee and ensure compliance of SHC clinical studies. You will report to the Clinical Research Program Manager and collaborate with SHC staff to safeguard subjects and data.

Responsibilities include tracking regulatory and IRB information, coordinating data collection and analysis, and upholding Belmont, GCP, and ethical standards while coordinating with leadership to advance SHC’s research mission.

Qualifications

• 5+ years of clinical research administration experience without a bachelor’s degree.
• 3+ years of clinical research experience with site management and IRBs.
• Knowledge of regulatory guidance for clinical research and data collection.
• Ability to learn electronic health systems and clinical research databases.

Responsibilities

• Maintain regulatory requirements knowledge and ensure study compliance.
• Track all aspects of projects including IRB information and recruitment activity.
• Coordinate data collection, statistical analysis, and dissemination of results.
• Prepare study results and ensure data integrity and privacy.
• Uphold Belmont Report, Nuremberg Code and ICH GCP standards.

Skills

Regulatory knowledge

Data management

Study coordination

IRB experience

Ethical standards

Education

Bachelor’s degree in Clinical Research or related field

Master’s degree in Clinical Research or related field

Tools

Electronic Health Records systems

Research databases

Job description

Company Overview

Shriners 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 Description

The Clinical Research Coordinator, Level 2 (CRC2) is a specialized, independent research professional who ensures oversight and compliance of both system-wideand 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 appropriatelycollect and safeguard data. Overall, the CRC is the site’s primary liaison among research participants, the localinvestigator(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 developmentto implementation
• Responsible for tracking all aspects of projects including all study, investigator and Institutional Review Board (IRB) information, patient recruitment activity, and financialmanagement
• Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study
• Contributes in compiling, critically analyzing and preparing study results to share with research team
• Demonstrates knowledge of ethical standards set forth by the Belmont Report, the Nuremberg Code and the International Conference of Harmonization GCP standards
• Maintains patient safety and privacy throughout the study
• Works effectively with SHC leadership to ensure the research mission is upheld
• Maintains scientific integrity, intellectual honesty, and excellence

Required Qualifications:

• Without a Bachelor’s degree, 5 or more years of specific job-related experience in the administration of clinical research is required
• 3 or more years of clinical research experience, e.g. experience with site management, study management, IRB’s, and federal regulationsregarding clinical research compliance
• Knowledge of, or ability to learn, electronic health system and databases used in research environments
• Working knowledge of regulation and guidance(s) related to clinical research
• Knowledge of, or ability to learn, participantand sample collection for large scale initiatives
• Working knowledge of the applicable regulations related to product or agentbeing studied, the specific protocol, the informed consent process, and the sponsors’ policies and procedures

Preferred Qualifications:

• Bachelor’s or Master’s Clinical Research, science or other health-carerelated field
• CCRP or CCRC certification
• Experience in the coordination of intergroup or multi-site clinical studies

The pay range for this position is $32.40 - $48.60/hour.

Compensation is determined based on years of relevant experience and departmental equity.