Senior Project Manager

Precision For Medicine

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

Posted 10/8/2026full-timeRemote • United StatesSenior💰 $147,300 - $220,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical research project management, including budget management, risk mitigation, and compliance with ICH-GCP standards. Proven ability to lead cross-functional teams and communicate effectively with clients and stakeholders.

Highest-signal resume keywords

Clinical Research ExperienceProject Management ExperienceBudget ManagementRisk ManagementETMF and EDC Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project PlanningChange ManagementStrategic PlanningRisk ManagementClinical Trial ManagementOncology ResearchGene Therapy KnowledgePharmaceutical ResearchData AnalysisQuality Management

Soft Skills

Communication SkillsInterpersonal SkillsOrganizational SkillsAttention to DetailNegotiation Skills

Tools & Technologies

Microsoft Office ProductsMicrosoft ProjectETMFEDCCTMS

Industry Keywords

ICH-GCPClinical Study ManagementCross-Functional ManagementGlobal TrialsStudy Team Leadership

About the role

Key responsibilities & impact

Plan, direct, coordinate, and deliver activities for designated clinical study projects to achieve quality, scope, cost, and time objectives
Serve as primary point-of-contact and escalation point to the client
Coordinate and oversee functional services and external vendors according to established timelines and budgets
Manage study budgets, scope, out-of-scope activities, change orders, and project financial health
Collaborate with clinical operations and functional teams in study delivery and clinical activities
Develop comprehensive 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 progress, KPIs, solutions, and opportunities to clients and senior management
Lead internal and client meetings and set expectations for project teams
Communicate protocol/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 travel to bid defense meetings
Perform other duties assigned by management
Remain compliant with organizational training, time-reporting, and administrative requirements
Provide ongoing feedback and annual performance reviews for functional team members

Requirements

What you’ll need

Bachelor’s degree or equivalent combination of education/experience in science or health-related field (North America)
Degree or equivalent combination of education/experience in science or health-related field (EU)
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 in 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 effectively interface with others in a team setting
Proven organizational skills, attention to detail, and a customer service demeanor
Demonstrates knowledge of ICH-GCP and relevant Precision SOPs, as well as the ability to implement such items
Direct work experience in a global, cross-functional project management environment
Good understanding of cross-functional management
Good understanding of project planning, risk management and change management with an awareness of appropriate escalation
Proven experience in strategic 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
Ability to create an environment where study team members have a sense of ownership
Results oriented, accountable, motivated and flexible
Proven time management, negotiation, critical thinking, decision making, analytical and interpersonal skills
Proven presentation, verbal and written communications skills
Good understanding of project management software
In depth proven experience in pharmaceutical and/or device research required
Experience with oncology & 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