Clinical Research Assistant, Oncology Trials & Phlebotomy
Overview
Onsite clinical research role supporting oncology trials at multiple LA area sites. Own patient visits, data collection, and regulatory tasks to enable study progress on ~45 active trials. This developmental position offers a clear path toward a Clinical Research Coordinator role within a collaborative team.
What You'll Do10
- 1Build patient visit workflows, coordinate visits, and ensure a compassionate patient experience
- 2Design data capture steps and enter study data accurately to support data integrity
- 3Lead phlebotomy, vital signs, and ECGs during study visits in accordance with protocols
- 4Ship regulatory documentation and support submissions to regulatory bodies and CROs
- 5Own chart reviews and pre-screening to support timely enrollment
- 6Drive data quality by addressing queries in EDC systems and aligning with data management
- 7Collaborate with data management and regulatory teams to maintain compliance
- 8Support study communications with sponsors and vendors to keep trials on track
- 9Scale operational processes across multiple sites to support growth
- 10Assist with travel logistics to designated sites for patient visits
Requirements10
- 11 year of experience as a Clinical Research Coordinator or closely related role
- 2Hands-on experience supporting patient visits in clinical studies
- 3Demonstrated ability to perform phlebotomy, measure vital signs, and conduct ECGs
- 4Proficiency in chart review and pre-screening for trial eligibility
- 5Experience in oncology trials and data collection with attention to detail
- 6Certified Phlebotomist with demonstrated competency
- 7Ability to travel between multiple clinical sites as required
- 8Strong communication and interpersonal skills for multidisciplinary teams
- 9Excellent organizational skills and ability to follow structured schedules
- 10Comfort working in a fast-paced environment with multiple oncology trials
Salary Insight
$42 - $52k per year
Location
Required Skills
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