Redeployment
Clinical Research Coordinator II
Pay: $38.00/hr – $44.00/hr (DOE)
Employment type: Independent Contractor (1-month temporary assignment)
Location: Long Beach, CA
A leading clinical research organization operating multiple community-based trial sites across Southern California. The team conducts high-quality, ethical clinical studies across therapeutic areas with a focus on public health impact and regulatory compliance.
The Clinical Research Coordinator II will provide specialized support for multiple vaccine clinical trials during a high-enrollment period. This is a one-month contract position requiring strong vaccine trial coordination skills and experience managing complex vaccination protocols, safety assessments, and participant oversight in a regulated research setting.
What You’ll Do
Coordinate daily activities for Phase I–IV preventive and therapeutic vaccine studies
Screen, consent, and enroll participants according to vaccine-specific inclusion and exclusion criterial>
Manage vaccine administration visits and oversee post-vaccination observation periods
Monitor participants for adverse reactions and complete follow-up safety evaluations
Maintain vaccine storage, handling, and accountability logs in compliance with protocol and cold chain requirements
Document vaccination records, adverse events, and safety data accurately within clinical databases
Coordinate specimen collection for immunogenicity and safety laboratory assessments
Schedule participant follow-up visits and safety phone calls per protocol timelines
Support preparation for sponsor monitoring visits and regulatory inspections
Ensure compliance with Good Clinical Practice (GCP), FDA, and ICH regulations throughout all study activities
Qualifications Required:
Minimum 3 years of clinical research coordination experience
At least 2 years of direct vaccine clinical trial experience
Proficiency in vaccine administration, handling, and cold chain management
Strong understanding of post-vaccination safety monitoring and adverse event reporting
Current certification from ACRP or SOCRA strongly preferred
Bachelor’s degree in nursing, life sciences, or a related healthcare field
Proficiency with electronic data capture (EDC) and clinical trial management systems (CTMS)
Comprehensive knowledge of GCP, FDA regulations, and vaccine safety standards
Immediate availability for a 1-month assignment with a full-time schedule (6 days per week)
Valid California driver’s license and reliable transportation
Preferred:
Prior experience in COVID-19, influenza, or other preventive vaccine trials
Familiarity with VAERS (Vaccine Adverse Event Reporting System)
Background in high-volume enrollment trial environments
Bilingual English/Spanish communication skills
About The Company. This organization is a community-focused clinical research network dedicated to advancing medical science through ethical, patient-centered studies. With expertise in vaccine development and large-scale enrollment management, it contributes to public health improvement through rigorous, compliant, and innovative research practices.
#J-18808-Ljbffr
A leading clinical research organization operating multiple community-based trial sites across Southern California. The team conducts high-quality, ethical clinical studies across therapeutic areas with a focus on public health impact and regulatory compliance.
The Clinical Research Coordinator II will provide specialized support for multiple vaccine clinical trials during a high-enrollment period. This is a one-month contract position requiring strong vaccine trial coordination skills and experience managing complex vaccination protocols, safety assessments, and participant oversight in a regulated research setting.
What You’ll Do
Coordinate daily activities for Phase I–IV preventive and therapeutic vaccine studies
Screen, consent, and enroll participants according to vaccine-specific inclusion and exclusion criterial>
Manage vaccine administration visits and oversee post-vaccination observation periods
Monitor participants for adverse reactions and complete follow-up safety evaluations
Maintain vaccine storage, handling, and accountability logs in compliance with protocol and cold chain requirements
Document vaccination records, adverse events, and safety data accurately within clinical databases
Coordinate specimen collection for immunogenicity and safety laboratory assessments
Schedule participant follow-up visits and safety phone calls per protocol timelines
Support preparation for sponsor monitoring visits and regulatory inspections
Ensure compliance with Good Clinical Practice (GCP), FDA, and ICH regulations throughout all study activities
Qualifications Required:
Minimum 3 years of clinical research coordination experience
At least 2 years of direct vaccine clinical trial experience
Proficiency in vaccine administration, handling, and cold chain management
Strong understanding of post-vaccination safety monitoring and adverse event reporting
Current certification from ACRP or SOCRA strongly preferred
Bachelor’s degree in nursing, life sciences, or a related healthcare field
Proficiency with electronic data capture (EDC) and clinical trial management systems (CTMS)
Comprehensive knowledge of GCP, FDA regulations, and vaccine safety standards
Immediate availability for a 1-month assignment with a full-time schedule (6 days per week)
Valid California driver’s license and reliable transportation
Preferred:
Prior experience in COVID-19, influenza, or other preventive vaccine trials
Familiarity with VAERS (Vaccine Adverse Event Reporting System)
Background in high-volume enrollment trial environments
Bilingual English/Spanish communication skills
About The Company. This organization is a community-focused clinical research network dedicated to advancing medical science through ethical, patient-centered studies. With expertise in vaccine development and large-scale enrollment management, it contributes to public health improvement through rigorous, compliant, and innovative research practices.
#J-18808-Ljbffr