Onyx Bio · 14 hours ago
Clinical Research Coordinator
United States
Contract
Remote
Entry, Mid Level
$30/hr - $40/hr
2+ years expOnyx Bio is building a virtual immune system to advance precision medicine through AI-driven insights. They are seeking a remote Clinical Research Coordinator to manage decentralized clinical research activities across autoimmune studies, ensuring protocol adherence and high-quality data collection.
Biotechnology
Hiring Manager
Amit Lakhani
Responsibilities
Recruit, screen, and enroll research members into Onyx studies using remote channels (digital campaigns, referrals, online communities, virtual outreach)
Conduct virtual informed consent discussions and manage e‑consent workflows to ensure understanding of procedures, risks, and rights
Coordinate all remote study activities, including telehealth visits, digital surveys, remote biospecimen logistics (if applicable via third‑party vendors), and ongoing virtual follow‑up
Collect and organize remote clinical data and real‑world evidence, including uploaded health records, ePROs, and member‑reported outcomes via digital platforms
Monitor protocol adherence and visit windows using remote tracking tools; document adverse events and concomitant medications based on member reports and records
Maintain accurate and complete electronic study documentation, including source notes, case report forms, and digital regulatory binders
Support IRB submissions, amendments, and continuing reviews with remotely managed documents, reports, and member‑facing materials
Collaborate virtually with data, product, and operations teams to troubleshoot remote workflows and ensure data quality in decentralized studies
Qualification
Required
Bachelor's degree in a related field (life sciences, public health, or similar)
2–4+ years as a Clinical Research Coordinator or similar role, ideally with longitudinal or registry/observational studies
Demonstrated experience managing participant scheduling, consent, follow‑up, and data collection across multiple timepoints
Working knowledge of GCP, HIPAA, and IRB requirements for human subjects research; prior completion of GCP/CITI or equivalent
Proven ability to work independently in a remote setting, prioritize tasks, and manage a large longitudinal participant panel
Excellent interpersonal skills and comfort conducting virtual consent discussions and check‑ins via video/phone
Preferred
Experience with decentralized or hybrid studies (remote consent, at‑home data collection, digital engagement)
Background in autoimmune disease research, biobanks, registries, or multiomics cohorts
Prior work in a startup, biotech, or digital health company
Company
Onyx Bio
Onyx is building a virtual immune system for faster and safer development of precision medicines.
2-10 employees
Funding
Current Stage
Early StageCompany data provided by crunchbase