Remote Oncology Clinical PM | Global Trials Lead

Ladders; United States; Remote; USD 120,000 - 135,000; Full time

Benefits offered by this job

Health benefits: medical

Dental and Vision

401(k) match

Employee Stock Purchase Plan

Job summary

Ladders is seeking a Clinical Project Manager for Oncology in a sponsor-dedicated, remote setting. You will drive global oncology trials, partner with Study Leads, and coordinate cross-functional teams to keep studies on track from startup to closeout.

The role requires strong study management discipline, vendor coordination, and the ability to report to executives while maintaining timelines and mitigating risks.

Qualifications

• Bachelor's degree in a scientific, healthcare, or related field is required.
• 3+ years of Clinical Project Management experience supporting global oncology trials.
• Experience managing studies across multiple countries and regions.
• Vendor management experience is required.
• Strong understanding of clinical trial operations and lifecycle management.
• Strong knowledge of ICH-GCP guidelines and clinical research regulations.

Responsibilities

• Support Clinical Study Leads and cross-functional study teams on global oncology trials.
• Lead day-to-day study management activities including startup, conduct, maintenance, and closeout.
• Manage study timelines, deliverables, risks, and issue resolution.
• Oversee external vendors, including CROs and specialty providers.
• Coordinate Clinical Trial Team meetings and drive action item follow-up.
• Monitor study performance metrics and identify areas needing intervention.
• Contribute to study status reporting and executive communications.

Skills

Clinical Project Management

Vendor management

Global oncology trials

ICH-GCP knowledge

Cross-country experience

Education

Bachelor's degree in a scientific/healthcare field

Job description

Ladders is seeking a Clinical Project Manager for Oncology in a sponsor-dedicated, remote setting. You will drive global oncology trials, partner with Study Leads, and coordinate cross-functional teams to keep studies on track from startup to closeout.

The role requires strong study management discipline, vendor coordination, and the ability to report to executives while maintaining timelines and mitigating risks.