Project Director – Oncology

Precision For Medicine

. Serve as primary point-of-contact liaison with clients, including proposal activities and client presentations .

Posted 10/23/2026full-timeRemote • United StatesLead💰 $162,000 - $243,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical research management, including oversight of project planning, execution, and compliance with ICH-GCP standards. Proven ability to lead cross-functional teams, manage budgets, and communicate effectively with clients and stakeholders.

Highest-signal resume keywords

Clinical Research ExperienceProject Management ExperienceMicrosoft Office ProficiencyETMF KnowledgeICH-GCP Mastery

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ManagementProject PlanningBudget ManagementRisk ManagementKPI ReportingStudy ComplianceProtocol CommunicationPerformance ReviewChange Order ManagementStudy-Specific Training

Soft Skills

Client LiaisonMentoringCommunicationLeadershipTeam Collaboration

Tools & Technologies

Microsoft ProjectETMFEDCCTMSMicrosoft OutlookMicrosoft WordMicrosoft ExcelMicrosoft PowerPoint

Industry Keywords

Pharmaceutical ResearchDevice ResearchGlobal StudiesBid Defense PreparationSOP Development

About the role

Key responsibilities & impact

Serve as primary point-of-contact liaison with clients, including proposal activities and client presentations
Oversee all aspects of clinical research trials and assigned portfolios
Direct project managers through project establishment, planning, initiation, procurement, execution and closing
Manage study budgets, scope, change orders and financial health
Develop or oversee comprehensive project plans, timelines, risk management and mitigation
Ensure quality management, eTMF inspection readiness and corrective/preventive action plans
Establish tracking metrics and monitor trial and team progress
Prepare project status updates, KPI reports and presentations for clients and senior management
Lead internal and client meetings and drive program or study-level strategies
Oversee cross-functional project teams and trial execution
Communicate protocol/study issues and implement necessary actions
Conduct formal presentations, including bid defenses
Ensure study-specific training and compliance
Support business development and marketing activities, including bid defense preparation and travel
Mentor associate, project and senior project managers
Participate in departmental updates and company SOP development
Provide ongoing feedback and annual performance reviews for functional team members
Identify project-level performance problems and ensure corrective action
Complete organizational training, time reporting and administrative duties
Travel domestically and internationally as required

Requirements

What you’ll need

Bachelor’s degree or equivalent combination of education/experience in science or health-related field (North America)
Minimum of 8 years of clinical research experience or proven competencies for this position
Minimum of 5 years of direct project management experience
High proficiency with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS
Experience managing highly complex and global studies or a portfolio of studies
Mastery knowledge of ICH-GCP and relevant Precision SOPs
Highly experienced in pharmaceutical and/or device research
Ability to travel domestically and internationally, including overnight stays
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