Clinical Research Coordinator
$72,800–$99,840 year
On-site · Murrieta, California, United States
Job Summary
Clinical Research Coordinator at Flourish Research (Murrieta, CA) supporting oncology trials across Phase I–IV. Responsibilities include executing protocol-specified patient visits/procedures (phlebotomy, IVs, injections, vital signs, ECG/EKG), managing source data and CRFs/eCRFs, obtaining informed consent, ethically recruiting subjects to meet enrollment timelines, ongoing training, coordinating visits per protocol, ensuring HIPAA/privacy, reporting AEs/SAEs, managing study materials, and collaborating with Leads, Managers, PIs/Sub-Is, and sponsors. Requires oncology clinical research experience, minimum two years, and familiarity with FDA/GCP/ICH; educational background preferably a Bachelor's degree; strong organizational, communication, and interpersonal skills; proficiency with computers and MS Office.
Required Qualifications
- Bachelor's degree preferred, but not required
- Must have oncology clinical research experience
- Minimum of two years of clinical research experience
- Clinical skills: vital signs, EKG/ECG, phlebotomy, injections
- Familiar with e-source reporting via an electronic platform
- Understanding of ICH, FDA, and GCP regulations
- Impeccable organizational skills and attention to detail
- Excellent communication and interpersonal skills to interact with PI, study team, sponsor/CROs, potential subjects
- Ethical compass; detail-oriented; self-driven
Desired Qualifications
- Bachelor's degree preferred
- oncology clinical research experience
- minimum of two years clinical research experience
- Familiar with e-source reporting via an electronic platform
- Impeccable organizational skills and attention to detail
- Excellent communication and interpersonal skills
- Proficiency with computers and Microsoft Office Suite
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