SoTalent
Location:
Orange, CA
Estimated Salary:
$60,000–$72,000 annually
Employment Type:
Full-time, Onsite
The Opportunity A leading
healthcare and research organization
is seeking a
Clinical Research Coordinator
to oversee the day‑to‑day operations of multiple clinical research studies. This role plays a critical part in ensuring study integrity, regulatory compliance, and seamless coordination between investigators, patients, sponsors, and regulatory bodies.
You’ll work closely with the Principal Investigator to ensure strict adherence to study protocols and Good Clinical Practice (GCP/ICH) standards, while maintaining accurate, timely documentation across all studies.
What You’ll Do
Coordinate and manage daily operations of multiple clinical research studies
Serve as the primary liaison between the Principal Investigator, patients, sponsors, and the Institutional Review Board (IRB)
Ensure all study documentation is accurate, complete, and submitted on time
Support compliance with study protocols, GCP/ICH guidelines, and regulatory requirements
Assist with patient coordination and study‑related procedures as required
Maintain organized research files and support audits and inspections
Key Responsibilities
Monitor study progress and ensure protocol adherence
Coordinate communication across internal and external research stakeholders
Maintain regulatory binders and study documentation
Support data integrity and quality control initiatives
Assist with biohazard material handling and sample logistics where applicable
What You Bring
Completion of an accredited Medical or Phlebotomy training program, or equivalent education/experience
2+ years of experience in a clinical research setting (3 years preferred)
Working knowledge of clinical trial operations and regulatory standards
Strong organizational skills with exceptional attention to detail
Ability to manage multiple studies simultaneously in a fast‑paced environment
Clear, professional communication skills
Preferred Qualifications
College degree or vocational school graduate
Biohazardous materials packaging training
Experience working in hospital- or clinic‑based clinical research environments
Why This Role This position offers the opportunity to contribute to meaningful clinical research within a
patient‑centered healthcare environment , while gaining exposure to complex studies, multidisciplinary teams, and long‑term career growth in clinical research.
Seniority Level Associate
Employment Type Full‑time
Job Function Research
Industries Health and Human Services
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Orange, CA
Estimated Salary:
$60,000–$72,000 annually
Employment Type:
Full-time, Onsite
The Opportunity A leading
healthcare and research organization
is seeking a
Clinical Research Coordinator
to oversee the day‑to‑day operations of multiple clinical research studies. This role plays a critical part in ensuring study integrity, regulatory compliance, and seamless coordination between investigators, patients, sponsors, and regulatory bodies.
You’ll work closely with the Principal Investigator to ensure strict adherence to study protocols and Good Clinical Practice (GCP/ICH) standards, while maintaining accurate, timely documentation across all studies.
What You’ll Do
Coordinate and manage daily operations of multiple clinical research studies
Serve as the primary liaison between the Principal Investigator, patients, sponsors, and the Institutional Review Board (IRB)
Ensure all study documentation is accurate, complete, and submitted on time
Support compliance with study protocols, GCP/ICH guidelines, and regulatory requirements
Assist with patient coordination and study‑related procedures as required
Maintain organized research files and support audits and inspections
Key Responsibilities
Monitor study progress and ensure protocol adherence
Coordinate communication across internal and external research stakeholders
Maintain regulatory binders and study documentation
Support data integrity and quality control initiatives
Assist with biohazard material handling and sample logistics where applicable
What You Bring
Completion of an accredited Medical or Phlebotomy training program, or equivalent education/experience
2+ years of experience in a clinical research setting (3 years preferred)
Working knowledge of clinical trial operations and regulatory standards
Strong organizational skills with exceptional attention to detail
Ability to manage multiple studies simultaneously in a fast‑paced environment
Clear, professional communication skills
Preferred Qualifications
College degree or vocational school graduate
Biohazardous materials packaging training
Experience working in hospital- or clinic‑based clinical research environments
Why This Role This position offers the opportunity to contribute to meaningful clinical research within a
patient‑centered healthcare environment , while gaining exposure to complex studies, multidisciplinary teams, and long‑term career growth in clinical research.
Seniority Level Associate
Employment Type Full‑time
Job Function Research
Industries Health and Human Services
#J-18808-Ljbffr