Arbor

Clinical Research

• Lead day-to-day clinical trial operations across assigned studies, sites, CROs, laboratories, and vendors
• Manage study start-up, site activation, monitoring oversight, and close-out activities
• Own and manage study timelines, budgets, invoices, vendor deliverables, and key milestones
• Oversee study documentation and trial master file quality to support inspection readiness
• Review and provide operational leadership on clinical documents, including protocols, ICFs, CRFs, SAPs, CSRs, study plans, and related materials
• Partner with cross-functional study teams to drive study execution, resolve operational issues, and support study milestones
• Manage clinical sample logistics between patients, sites, and laboratory vendors
• Drive timelines and logistics for Safety Review Boards, Data Monitoring Committees, data cuts, and related study activities
• Lead or support vendor review, selection, contracting, onboarding, and performance oversight
• Build and manage relationships with investigative sites, CROs, vendors, clinical experts, and internal stakeholders, including planning investigator meetings
• Identify, escalate, and resolve study risks and operational issues
• Represent the company externally with study partners and investigative sites
• Travel domestically and internationally to investigative sites or study-related meetings as needed

Explore Senior Clinical Trial Manager at Arbor. Review requirements and application details.