Senior Oncology Clinical Project Manager - Phase 3, Remote

UBC; United States; À distance; USD 150 000 - 210 000; Plein temps

Avantages offerts par ce poste

Remote opportunities

Growth opportunities for promotion

401K with company match*

Flexible work environment

Discretionary PTO

Paid Holidays

Employee assistance programs

Medical, Dental, and vision coverage

HSA/FSA

Wellness program

Adoption assistance

Short term disability

Long term disability

Life insurance

Résumé du poste

UBC seeks a Senior Clinical Project Research Manager to lead oncology Phase 3 studies from start-up through close-out in a remote United States setting. You will coordinate cross-functional teams, manage sponsor relationships, and drive on-time milestones while ensuring regulatory compliance and audit-ready documentation.

Responsibilities include budget oversight, investigator meetings, mentoring PMs, process improvements, and revenue management for multiple projects.

Qualifications

• BA Degree or minimum 5 years of direct project management experience at a CRO or proven leadership/management experience.
• Excellent supervisory skills.
• Excellent interpersonal skills.
• Excellent presentation skills.
• Ability to independently assess issues and/or mitigate risk by using critical judgment to come to a resolution.
• Very good knowledge of regulatory requirements (i.e. Good Clinical Practice, ICH guidelines, etc.).
• 10% travel.

Responsabilités

• Serve as the primary sponsor contact for all study items, with oversight of all aspects of project conduct through close-out per SOPs, budgets, timelines and contracts.
• Execute operational aspects of assigned project activities and special projects.
• Assist in development and design of protocols, CRFs, regulatory documents, project master file, and other deliverables.
• Develop and monitor operational plans including communication, monitoring, project plans, training, timelines, and compliance; monitor progress against plans.
• Facilitate and plan investigator meetings; recruit qualified investigators and assist in budget negotiations.
• Supervise APM/PMs and other team members; provide reports to Sponsor on project progress.
• Lead projects with cross-functional involvement and supervise all supporting functions.
• Assist in revenue and invoicing for project(s).
• Ensure project training occurs and assist with training for project.
• Serve as a resource for inquiries and issue resolution for site management, contract budget, and regulatory document preparation.
• Lead internal client teleconferences/meetings and present project information at client meetings, bid defenses and monthly project review meetings.
• Maintain project documentation to be audit-ready.
• Support APM/PMs in sponsor/regulatory audits as required.
• Assist in preparation of client proposals in response to RFPs.
• Ensure project budget is tracked against contract milestones.
• May assist in protocol development and/or patient/subject consent form or REMS documents as required.
• Initiate and lead process improvement activities.
• Accurate reporting and interpretation of project metrics.
• Proposal and implementation of action plans.
• Satisfactory delivery of contracted services and milestones for assigned projects.
• Duties described for Project Manager and other duties as assigned by management.

Connaissances

Supervisory skills

Interpersonal skills

Presentation skills

Issue resolution

Regulatory knowledge

Travel readiness

Formation

BA Degree or equivalent

Description du poste

UBC seeks a Senior Clinical Project Research Manager to lead oncology Phase 3 studies from start-up through close-out in a remote United States setting. You will coordinate cross-functional teams, manage sponsor relationships, and drive on-time milestones while ensuring regulatory compliance and audit-ready documentation.

Responsibilities include budget oversight, investigator meetings, mentoring PMs, process improvements, and revenue management for multiple projects.