Remote Global Oncology Clinical Project Manager

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

Benefits offered by this job

Health benefits

401k with company match

Employee stock purchase plan

Fully remote (US)

Flexible scheduling

Paid time off & sick leave

Dental & Vision

Job summary

Ladders is seeking a Clinical Project Manager - Oncology for a fully remote, US-based role dedicated to sponsor-led oncology programs. You will drive daily study management from startup to closeout, coordinate with cross-functional teams, vendors and CROs, and monitor timelines, risks and performance to optimize global development programs.

The role requires 3+ years in global oncology trial management, strong operations understanding, and vendor oversight in a sponsor-dedicated environment.

Qualifications

• Bachelor's degree in a scientific or healthcare field.
• 3+ years of Clinical Project Management experience in global oncology trials.
• Experience managing studies across multiple countries and regions.
• Vendor management experience essential.
• Strong grasp of clinical trial operations and lifecycle management.
• Familiarity with ICH-GCP guidelines and clinical research regulations.
• Proficiency with Microsoft Office Suite.

Responsibilities

• Support Clinical Study Leads and cross-functional teams on oncology trials.
• Lead daily study management activities from startup to closeout.
• Manage study timelines, deliverables, and risks while resolving issues.
• Oversee external vendors and CROs.
• Coordinate Clinical Trial Team meetings and track action items.
• Contribute to study-level planning and operational strategy execution.
• Monitor study performance metrics and identify areas for improvement.

Skills

Oncology trial operations

Global trial execution

Vendor management

ICH-GCP knowledge

Study lifecycle management

Regulatory compliance

MS Office proficiency

Education

Bachelor's degree in science/healthcare

Job description

Ladders is seeking a Clinical Project Manager - Oncology for a fully remote, US-based role dedicated to sponsor-led oncology programs. You will drive daily study management from startup to closeout, coordinate with cross-functional teams, vendors and CROs, and monitor timelines, risks and performance to optimize global development programs.

The role requires 3+ years in global oncology trial management, strong operations understanding, and vendor oversight in a sponsor-dedicated environment.