Clinical Research Coordinator II / Full-time / Days
About The Position
Position Summary: The Clinical Research Coordinator II, as a certified research professional, handles clinical trial administration for all protocol phases. Children's Hospital Los Angeles is seeking a Clinical Research Coordinator II (CRC II) to support an innovative study aimed at improving survivorship care transitions for young adult childhood cancer survivors (CCS), particularly those experiencing health-related social needs (HRSN). This position is ideal for a certified research professional with experience in clinical trials involving pediatric, adolescent, and young adult populations, and a strong commitment to advancing health equity. The CRC II will be responsible for ensuring regulatory compliance, maintaining high-quality data, and facilitating effective communication among study participants, healthcare providers, and key stakeholders. Will serve as a resource for study team members and principal investigators and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Assists in quality assurance/control of data resulting from studies. Provides cross-coverage for other CRCs within the department. Finally, the CRC II will contribute to the study's implementation and evaluation using the RE-AIM framework.
Requirements
- 3+ year experience in clinical trial coordination with 1+ years pediatric clinical trials experience.
- Strong organizational skills
- Experience in clinical trials involving pediatric, adolescent, and young adult populations
- Bachelor's degree or associates degree in related scientific field.
- ACRP Certified Clinical Research Coordinator (CCRC) or SOCRA Certified Clinical Research Professional (CCRP). Candidates with a medical degree are exempt from certification requirement.
Responsibilities
- Ensuring regulatory compliance
- Maintaining high-quality data
- Facilitating effective communication among study participants, healthcare providers, and key stakeholders
- Serve as a resource for study team members and principal investigators
- Assists with subject recruitment
- Data collection
- Scheduling of study-related activities and follow-up with enrolled subjects
- Assists in quality assurance/control of data resulting from studies
- Provides cross-coverage for other CRCs within the department
- Contribute to the study's implementation and evaluation using the RE-AIM framework
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Industry
Hospitals
