Remote Oncology Clinical Project Manager, Global Trials

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

Benefits offered by this job

Flexible remote work

Health benefits

401k match

Employee stock purchase plan

Job summary

The Ladders seeks a Clinical Project Manager - Oncology (Remote) to oversee global oncology studies from startup to closeout, focusing on timelines, issue resolution, and quality. You will collaborate with Clinical Study Leads, vendors, and CROs across regions to keep trials moving forward.

Key responsibilities include coordinating study startup, conduct, maintenance, and closeout, managing timelines and risks, and supporting operational strategies to advance cancer therapies.

Qualifications

• Bachelor's degree in a scientific/healthcare field.
• 3+ years of CPM experience in global oncology trials.
• Experience across NA, Europe, Asia-Pacific.
• Vendor management and CRO oversight.
• Solid knowledge of ICH-GCP guidelines and regulations.
• Experience in Phase I–IV oncology studies.

Responsibilities

• Support Clinical Study Leads and cross-functional teams in global oncology trials.
• Lead day-to-day startup, conduct, maintenance, and closeout.
• Manage study timelines, deliverables, risks, and issues.
• Oversee external vendors and CROs involved in clinical trials.
• Coordinate Clinical Trial Team meetings and ensure follow-up on action items.
• Support planning and execution of operational strategies for studies.
• Monitor and assess study performance metrics, addressing issues proactively.

Skills

Clinical project management

Global oncology trials

Vendor management

ICH-GCP knowledge

Regulatory compliance

Education

Bachelor's degree in science/healthcare

Job description

The Ladders seeks a Clinical Project Manager - Oncology (Remote) to oversee global oncology studies from startup to closeout, focusing on timelines, issue resolution, and quality. You will collaborate with Clinical Study Leads, vendors, and CROs across regions to keep trials moving forward.

Key responsibilities include coordinating study startup, conduct, maintenance, and closeout, managing timelines and risks, and supporting operational strategies to advance cancer therapies.