Clinical Trial Manager

Why Work With Us?

Our Science: Advancing Cancer Immunotherapies

Position Summary:

What You’ll Do:

• Provide operational management and leadership to cross-functional study team to execute the clinical study per agreed upon timelines, budget and quality.
• Drive startup through closeout: IRB, contracting, site selection, initiation, monitoring, and metrics tracking.
• Support inspection readiness and contribute to critical regulatory milestones.
• Co-monitor with CRAs; review site visit reports and escalate issues proactively.
• Maintain essential documents and trial master file (TMF) accuracy.
• Collaborate with internal teams and vendors to ensure alignment and effective execution.

What You Bring:

• 4+ years of CTM or site management experience in oncology clinical trials is required
• Deep understanding of Phase 3 trial conduct and in-house operational models
• Familiarity with ICH/GCP, FDA/EMA guidelines, and regulatory best practices
• Strong leadership and problem-solving skills; ability to manage ambiguity and prioritize independently
• Exceptional communication skills and comfort interacting with senior stakeholders
• Prior CRA experience is a plus
• High emotional intelligence and a “scrappy but humble” mindset

Why You’ll Succeed at Candel:

• You know how to get things done without needing step-by-step instructions
• You value collaboration over ego and strive to lift others as you grow
• You’re excited to join a growing company and make a tangible impact
• You care about patients, science, and people—in that order

Work Environment: