Benefits:
401(k)
401(k) matching
Competitive salary
Dental insurance
Health insurance
Paid time off
Vision insurance
Orso Health is a leading organization in clinical research, dedicated to advancing healthcare through innovative studies. We are committed to excellence in research and invite you to be part of our dynamic team. California and the Arizona market. Known for our high standard of excellence, we are committed to providing compassionate, patient-centered care for both pediatric and adult patients. Our dedicated team strives to improve lives through the expert diagnosis and treatment of a wide range of allergy and asthma conditions. We are looking for high-energy, kind, and collaborative individuals who are eager to grow personally and professionally to join our team.
We are seeking a detail-oriented and proactive Clinical Research Associate (Part-Time) to monitor clinical study data and ensure the integrity and quality of research processes. The CRA will play a key role in supporting our Quality Assurance team by verifying data accuracy, compliance with study protocols, and regulatory requirements. Additionally, the CRA will assist in handling external monitoring visits to ensure smooth and compliant site audits.
This position requires minimal travel, with occasional support at our Los Angeles clinic sites in Torrance and Long Beach. Part-time employees must be available to work a minimum of 20 hours per week.
Key Responsibilities:
Monitor and review clinical study data for accuracy, completeness, and consistency throughout the study lifecycle.
Conduct site visits (remote or on-site) to review source documents, case report forms (CRFs), and other study documentation.
Assist in handling and coordinating external monitoring visits, including preparation, communication, and follow-up.
Collaborate with site staff and internal teams to resolve data discrepancies and ensure timely data entry.
Support the implementation and maintenance of quality assurance standards for clinical trials.
Assist in audit preparation and support regulatory inspections as needed.
Document monitoring activities in accordance with company SOPs and Good Clinical Practice (GCP) guidelines.
Contribute to continuous improvement initiatives to enhance data quality and compliance processes.
Additional duties as assigned.
Qualifications:
Bachelor’s degree in life sciences, healthcare, or related field.
Minimum of 5 years in clinical research monitoring or data management preferred.
Strong understanding of GCP, ICH guidelines, and clinical trial processes.
Excellent attention to detail and organizational skills.
Ability to communicate effectively with cross-functional teams and site staff.
Proficiency in CTMS, EDC systems, and Microsoft Office Suite.
Skills:
Analytical mindset with problem-solving skills.
Ability to prioritize tasks and manage time effectively.
Commitment to quality and regulatory compliance.
Job Type: Part-time
Benefits:
401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance