Clinical Project Manager - Oncology (Client Dedicated/Remote)

Ladders

United States

Remote

USD 120,000 - 135,000

Full time

6 hours ago
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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

For our client, we are seeking a Clinical Project Manager - Oncology (Client Dedicated/Remote) to join the team of a leader in the Healthcare space.

This remote role will oversee the day-to-day execution of global oncology studies from startup through closeout, with a strong focus on timeline management, issue resolution, and operational quality. The position partners closely with Clinical Study Leads, cross-functional internal teams, external vendors, and CROs to keep trials moving forward across multiple regions. Success in this role will support efficient study delivery, strong trial performance, and the advancement of innovative therapies for patients with cancer.

Location: Remote

Compensation: $120,000 – $135,000 annually

Responsibilities
  • Support Clinical Study Leads and cross-functional teams in global oncology trials
  • Lead day-to-day management of study startup, conduct, maintenance, and closeout
  • Manage study timelines, deliverables, risks, and issue resolution
  • 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
Qualifications
  • Bachelor's degree in a scientific, healthcare, or related field
  • 3+ years of Clinical Project Management experience in global oncology trials
  • Experience managing studies across multiple regions, including North America, Europe, and Asia-Pacific
  • Vendor management expertise
  • Strong understanding of clinical trial operations and lifecycle management
  • Experience with Phase I to Phase IV oncology studies
  • Firm knowledge of ICH-GCP guidelines and clinical research regulations
Benefits
  • Flexible remote work opportunity
  • Contribute to innovative oncology programs for cancer patients
  • Collaborative culture in a sponsor-dedicated team
  • Support cutting-edge therapies across various cancer types
  • Expand impact across global clinical development programs
  • Excellent health benefits including medical, dental, and vision
  • 401k company match and eligibility for employee stock purchase plan

Our client is an equal opportunity employer.

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