Senior Oncology Clinical Project Lead – Phase III/IV

UBC; Oregon; Hybrid; USD 110,000 - 170,000; Full time

Benefits offered by this job

Remote opportunities

Competitive salaries

Growth opportunities for promotion

401K with company match

Tuition reimbursement

Flexible work environment

Discretionary PTO

Paid Holidays

Employee assistance programs

Medical, Dental, and vision coverage

HSA/FSA

Telemedicine

Job summary

UBC in Oregon seeks a Senior Clinical Project Research Manager to lead cross-functional project teams and deliver milestones. You will serve as the sponsor’s primary point of contact, manage budgets and timelines, and ensure regulatory and SOP compliance across study phases.

This role requires strong leadership, excellent communication, risk mitigation, and the ability to mentor APM/PMs. You will coordinate investigator meetings, audit support, and client interactions while maintaining

Qualifications

• BA Degree or minimum 5 years of direct project management experience at a CRO or proven leadership/management experience.
• Excellent written verbal and non-verbal communication skills.
• Excellent supervisory skills.
• Excellent interpersonal skills.
• Excellent presentation skills.
• Ability to independently assess issues and mitigate risk by using critical judgment.

Responsibilities

• Serve as the primary contact with the sponsor for all study related items, with oversight of all aspects of project conduct from start-up through close-out.
• Execute operational aspects of assigned project activities and special projects.
• Assist in the development and design of protocols, CRFs, regulatory documents, and project deliverables.
• Ensure operational plans are aligned with project needs and monitor progress against plans.

Skills

Communication skills

Supervisory skills

Interpersonal skills

Presentation skills

Critical judgment

Risk management

Travel willingness

Education

BA degree

Job description

UBC in Oregon seeks a Senior Clinical Project Research Manager to lead cross-functional project teams and deliver milestones. You will serve as the sponsor’s primary point of contact, manage budgets and timelines, and ensure regulatory and SOP compliance across study phases.

This role requires strong leadership, excellent communication, risk mitigation, and the ability to mentor APM/PMs. You will coordinate investigator meetings, audit support, and client interactions while maintaining