Clinical Research Associate

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 standards 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. 

Position Summary

We are seeking a detail-oriented and proactive Clinical Research Associate 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, Long Beach, Scottsdale AZ. This role is non-exempt (hourly) and full-time, working 40 hours per week, Monday through Friday, Onsite in our La Jolla Clinic.

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.
  
  

Skills & Qualifications

• Education: Bachelor's degree in life sciences, healthcare, or related field.
• Experience: Minimum of 5 years in clinical research monitoring or data management preferred.
• Skills & Abilities:
• 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.
• Analytical mindset with problem-solving skills.
• Ability to prioritize tasks and manage time effectively.
• Commitment to quality and regulatory compliance.
  

Compensation

The hourly range for this position is $35.00-52.00/hour. The actual compensation for this role will be determined by a variety of factors, including but not limited to the candidate's skills, education, and experience.

Physical Requirements

Ability to stand, walk, and move throughout the clinic, if applicable, for extended periods; occasionally lift objects up to 25 lbs., bend, stoop, or reach as needed. Frequent use of hands and fingers for patient care and equipment operation. Must have normal (or corrected) vision and hearing and be able to respond quickly in a fast-paced clinical environment, if applicable.

What We Offer

• Competitive salary and benefits package, including medical, dental & vision insurance, 401(k) retirement plan with employer matching, and professional development opportunities
• In addition, we offer paid time Off (PTO), sick time, floating holiday and holiday pay
• Opportunity to shape the future of cutting-edge clinical research in beautiful San Diego (and across our expanding network)
• An opportunity to play an active role in medical advancement
  

If this role excites you, please submit your resume and a cover letter outlining your relevant experience and why you're passionate about joining our team. We look forward to hearing from enthusiastic candidates ready to drive our success!

California Consumer Privacy Act (CCPA) Notice

Orso Health ("OH") complies with the California Consumer Privacy Act ("CCPA"). Personal information provided in the job application process will be collected, used, and retained in accordance with applicable privacy laws. Candidates may request additional information regarding the categories of personal information collected and the purposes for which it is used during the hiring process.