ICON Plc
Clinical Research Associate - Oncology - Los Angeles
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Job Description
- Req#: JR141761
Employer Industry: Clinical Research
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Work remotely within the southeast region, with travel required for on-site monitoring visits
- Engage in meaningful work that contributes to patient safety and clinical research
- Collaborative work environment with cross-functional teams
- Competitive salary and benefits package
What to Expect (Job Responsibilities):
- Serve as the primary point of contact between investigational sites and the sponsor
- Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
- Ensure site compliance with ICH-GCP, SOPs, and regulations
- Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
- Document site progress and escalate risks or issues to the clinical team
What is Required (Qualifications):
- Bachelor's degree in Life Sciences or equivalent, or a qualified RN
- Eligible to work in the United States without visa sponsorship
- Minimum 2 years of on-site monitoring experience in the pharmaceutical or CRO industry
- Experience monitoring oncology trials
- Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
How to Stand Out (Preferred Qualifications):
- Willingness to travel up to 50% for on-site monitoring visits across the southeast region
- Preference for candidates residing in Los Angeles, CA, near major HUB airports to support efficient regional travel
#ClinicalResearch #OncologyTrials #CareerOpportunity #MonitoringExperience #PatientSafety
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