Oncology Clinical Project Manager II - Remote/Hybrid

Allucent; Oregon; Hybrid; USD 90,000 - 140,000; Full time

Benefits offered by this job

Flexible Working hours

Remote/hybrid possible

Training budget

Mentoring opportunities

Career progression

Spot Bonus Program

Loyalty Award Program

Job summary

Allucent is seeking a Project Manager II to lead global oncology clinical trials from start-up to delivery. You will manage cross-functional teams, ensuring studies stay on track, on budget, and compliant with GCP and regulatory requirements.

You will serve as the primary liaison for sponsors, vendors, and internal stakeholders. Join a fast-paced, collaborative environment focused on operational excellence, proactive risk management, and delivering high-quality clinical programs that meet client

Qualifications

• Minimum Bachelor's degree in life science, healthcare and/or business.
• Minimum 6 years of relevant work experience in drug development and/or clinical research.
• Minimum 1 year of project management experience as a clinical project manager.
• Experience managing Oncology programs, including global study execution and vendor oversight.

Responsibilities

• Lead cross-functional teams to deliver clinical trials on time, within scope, and on budget.
• Develop and execute project plans aligned with ICH-GCP, SOPs, and regulatory standards.
• Serve as the primary contact for sponsors, vendors, and internal stakeholders.
• Optimize vendor performance through strategic selection, management, and oversight.
• Mitigate risks and control budgets by addressing challenges and resource allocation.
• Maintain inspection-ready documentation including Trial Master File and study records.

Skills

Clinical trial management

Oncology programs

ICH-GCP knowledge

Budget/financial acumen

Bachelor's degree

Education

Bachelor's degree in life science, healthcare and/or business

Job description

Allucent is seeking a Project Manager II to lead global oncology clinical trials from start-up to delivery. You will manage cross-functional teams, ensuring studies stay on track, on budget, and compliant with GCP and regulatory requirements.

You will serve as the primary liaison for sponsors, vendors, and internal stakeholders. Join a fast-paced, collaborative environment focused on operational excellence, proactive risk management, and delivering high-quality clinical programs that meet client