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Precision Medicine Group

Project Director – Oncology

Precision Medicine Group

. Serve as the 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

Use this summary to align your resume positioning with the role.

Demonstrates extensive experience in clinical research management, including oversight of study portfolios, project planning, and risk management. Proficient in managing budgets and ensuring compliance with ICH-GCP and relevant SOPs while leading cross-functional teams and client communications.

Highest-signal resume keywords
Clinical Research ExperienceProject Management ExperienceMicrosoft Office ProficiencyETMF and EDC ProficiencyICH-GCP Knowledge

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Research ManagementProject PlanningRisk ManagementBudget ManagementChange ManagementCross-Functional Team LeadershipPerformance Metrics TrackingQuality ManagementProposal DevelopmentStudy Compliance
Soft Skills
Client CommunicationMentoringPresentation SkillsProblem-SolvingTeam Collaboration
Tools & Technologies
Microsoft ProjectETMFEDCCTMSMicrosoft OutlookMicrosoft WordMicrosoft ExcelMicrosoft PowerPoint
Industry Keywords
Pharmaceutical ResearchDevice ResearchSOP DevelopmentBid Defense PreparationStudy Execution

About the role

Key responsibilities & impact
  • Serve as the primary point-of-contact liaison with clients, including proposal activities and client presentations
  • Oversee all aspects of clinical research trials and assigned study portfolios
  • Direct project managers through project establishment, planning, initiation, procurement, execution and closing
  • Manage study budgets, scope, change orders and financial health, including profitability, billable hours, billing and forecasting
  • Develop or oversee comprehensive project plans, timelines, risk management and mitigation
  • 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 for clients and senior management, including KPIs and recommendations
  • Lead internal and client meetings and drive study-level strategies
  • Oversee cross-functional project teams and trial execution
  • Communicate protocol/study issues, deviations and required actions to sponsors and management
  • 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 project managers and provide performance feedback
  • Contribute to departmental updates and company SOP development
  • Identify project-level performance problems and ensure corrective action
  • Complete organizational training, time reporting and administrative duties
  • Perform other duties assigned by management

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
  • Highly proficient with Microsoft Office Products (Outlook, Word, Excel, PowerPoint)
  • Proficiency with 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
  • Knowledge of project management techniques and tools
  • Experience working in a cross-functional project management environment
  • Understanding of cross-functional management
  • Understanding of project planning, risk management and change management
  • 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