Job Description:
Location: Los Angeles, CA (90048)
Pay: $30 - $48/hour
Overview:
We are actively seeking a qualified and driven Clinical Research Coordinator to support and manage clinical trials across multiple sites. This role requires a hands-on, adaptable professional with strong clinical research experience, especially in the management of all aspects of trial operations and stakeholders, including PIs, patients, and sponsor/CRO representatives.
Key Responsibilities:
- Coordinate day-to-day activities for clinical research studies across various therapeutic areas (including, but not limited to, ophthalmology, dermatology, pulmonology), and at both HQ and satellite site locations
- Perform direct patient-facing duties, including informed consent, visit scheduling, and follow-up
- Manage all aspects of patient recruitment and enrollment across studies, including database reviews, outreach, pre-screening, and communications
- Confidently perform blood draws and handle biospecimen processing and shipping in accordance with protocol requirements
- Maintain and manage study documentation, source data, and regulatory binders across numerous systems, including CTMS, sponsor EDC systems, and more
- Support monitoring visits and participate in both internal and external audits
- Communicate effectively with sponsors, CROs, investigators, and internal departments
- Provide general support to the team and step in across functions as needed to meet study goals
Required Qualifications:
- Minimum 2 years of clinical research experience for industry-sponsored, interventional clinical trials for investigational drugs
- Proficiency in patient care, regulatory management, lab specimen handling, monitoring, and auditing
- Strong phlebotomy skills with confidence in blood draws
- Excellent multitasking, time management, and organizational abilities
- Willingness and ability to travel regularly (up to 50%) across sites
Preferred Qualifications:
- Fluent in Spanish (spoken and written)
- Certified Clinical Research Coordinator (CCRC) certification
- Prior experience with multi-site clinical trials or decentralized trial models
- Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms
- Background in therapeutic areas such as Ophthalmology, Dermatology, or Pulmonology