Senior Project Manager – Oncology

Precision For Medicine

. Plan, direct, coordinate, and deliver activities for designated clinical study projects to meet quality, scope, cost, and time objectives .

Posted 11/10/2026full-timeRemote • United StatesSenior💰 $147,300 - $220,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical project management, including managing complex global trials, developing project plans, and ensuring compliance with ICH-GCP standards. Proven ability to lead cross-functional teams, communicate effectively with stakeholders, and deliver projects within scope, budget, and timelines.

Highest-signal resume keywords

Clinical Research ExperienceProject Management ExperienceKnowledge of ICH-GCPExperience with eTMF and CTMSStrong Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project PlanningRisk ManagementChange ManagementBudget ManagementData AnalysisForecastingQuality ManagementStudy DesignPerformance MetricsTraining Compliance

Soft Skills

Interpersonal SkillsOrganizational SkillsAttention to DetailNegotiation SkillsCritical Thinking

Tools & Technologies

Microsoft Office ProductsMicrosoft ProjectETMFEDCCTMS

Industry Keywords

Pharmaceutical ResearchDevice ResearchOncologyCell TherapyGene Therapy

About the role

Key responsibilities & impact

Plan, direct, coordinate, and deliver activities for designated clinical study projects to meet quality, scope, cost, and time objectives
Serve as the primary client point of contact and escalation point
Coordinate and oversee functional services and external vendors according to timelines and budgets
Manage study budgets, scope, out-of-scope activities, financial health, profitability, billable hours, billing, and forecasting
Collaborate with clinical operations and functional teams in study delivery and clinical activities
Develop project plans, timelines, risk-management and mitigation strategies
Ensure quality management, eTMF inspection readiness, quality notifications, and corrective/preventive action plans
Establish tracking metrics for trial and team progress
Prepare project status updates and report KPIs and progress to clients and senior management
Lead internal and client meetings and set project-team expectations
Communicate study issues and deviations and implement necessary actions
Conduct formal presentations, including bid defenses
Implement and monitor study-specific training compliance
Support business development and marketing activities, including required bid-defense travel
Provide ongoing feedback and annual performance reviews for functional team members
Complete assigned duties, organizational training, time reporting, and administrative tasks

Requirements

What you’ll need

North America: Bachelor’s degree or equivalent combination of education/experience in science or health-related field; advanced degree preferred
EU: Degree or equivalent combination of education/experience in science or health-related field; advanced degree preferred
Minimum of 7 years of clinical research experience or proven competencies for this position
Minimum of 4 years of direct project management experience
Experience managing complex and global trials
Ability to travel domestically and internationally, including overnight stays
Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS
Proven communication and interpersonal skills to interface effectively with others in a team setting
Proven organizational skills, attention to detail, and customer service demeanor
Knowledge of ICH-GCP and relevant Precision SOPs
Direct work experience in a global, cross-functional project management environment
Understanding of cross-functional management
Understanding and proven experience in project planning, risk management and change management
High level of integrity and professional and ethical standards
Ability to lead and inspire excellence within a study team
Proven time management, negotiation, critical thinking, decision-making, analytical and interpersonal skills
Proven presentation, verbal and written communication skills
Understanding of project management software
In-depth proven experience in pharmaceutical and/or device research required
Experience with oncology and cell and/or gene therapy preferred
Candidates must be legally authorized to work in the country of employment without employer sponsorship

Benefits

Comp & perks

Discretionary annual bonus
Health insurance
Retirement savings benefits
Life insurance
Disability benefits
Parental leave
Paid time off for sick leave and vacation