Clinical Research RN (Cell Therapy / CAR-T) - High Paying
50–71 an hour
Behavioral Health Market Context
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Job Description
ssful candidate will report to the Clinical Research Manager and play a key role in managing study operations and ensuring compliance with regulatory and safety standards.
Responsibilities
• Coordinate and manage clinical research studies, ensuring adherence to protocols and regulatory requirements
• Administer and monitor advanced therapies, including cell therapy and CAR-T
• Perform patient assessments and collect clinical trial data using Electronic Data Capture (EDC), CTMS, and paper documentation
• Collaborate with physicians, research teams, and sponsors to support study execution
• Educate patients and families about study protocols and treatment processes
• Ensure safety monitoring and implement quality control measures throughout trials
• Maintain accurate and timely documentation in compliance with ethical and regulatory guidelines
Required Qualifications
• Active Registered Nurse (RN) license
• Active California RN License
• BLS certification (AHA)
Preferred Qualifications
• Minimum of 2 years clinical research nursing experience
• Experience with cell therapy and CAR-T therapy administration
• Knowledge of clinical trial management and regulatory compliance
• Strong skills in patient assessment, data documentation, and communication
• Ability to collaborate effectively within multidisciplinary teams
Company DescriptionLanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.
Responsibilities
• Coordinate and manage clinical research studies, ensuring adherence to protocols and regulatory requirements
• Administer and monitor advanced therapies, including cell therapy and CAR-T
• Perform patient assessments and collect clinical trial data using Electronic Data Capture (EDC), CTMS, and paper documentation
• Collaborate with physicians, research teams, and sponsors to support study execution
• Educate patients and families about study protocols and treatment processes
• Ensure safety monitoring and implement quality control measures throughout trials
• Maintain accurate and timely documentation in compliance with ethical and regulatory guidelines
Required Qualifications
• Active Registered Nurse (RN) license
• Active California RN License
• BLS certification (AHA)
Preferred Qualifications
• Minimum of 2 years clinical research nursing experience
• Experience with cell therapy and CAR-T therapy administration
• Knowledge of clinical trial management and regulatory compliance
• Strong skills in patient assessment, data documentation, and communication
• Ability to collaborate effectively within multidisciplinary teams
Company DescriptionLanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.
Qualifications
- •Active Registered Nurse (RN) license
- •Active California RN License
- •BLS certification (AHA)
Benefits
Responsibilities
- •The successful candidate will report to the Clinical Research Manager and play a key role in managing study operations and ensuring compliance with regulatory and safety standards
- •Coordinate and manage clinical research studies, ensuring adherence to protocols and regulatory requirements
- •Administer and monitor advanced therapies, including cell therapy and CAR-T
- •Perform patient assessments and collect clinical trial data using Electronic Data Capture (EDC), CTMS, and paper documentation
- •Collaborate with physicians, research teams, and sponsors to support study execution
- •Educate patients and families about study protocols and treatment processes
- •Ensure safety monitoring and implement quality control measures throughout trials
- •Maintain accurate and timely documentation in compliance with ethical and regulatory guidelines
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