Senior Clinical Project Manager, Analyst

Johnson & Johnson

Clinical Project Manager managing global clinical trial schedules, budgets, risks, and resources for Johnson & Johnson’s innovative medicines. Coordinating Planisware and MS Project plans across cross-functional teams.

Posted 8/13/2026full-timeBeerse • 🇧🇪 BelgiumSenior💰 €72,500 - €115,230 per yearWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in Project Management within Pharmaceutical and Healthcare industries, with a strong focus on managing integrated study schedules, budgets, and resource allocation. Proven ability to lead teams, facilitate decision-making, and ensure compliance with clinical trial governance.

Highest-signal resume keywords

Project ManagementClinical Research OperationsBudget ManagementLeadership SkillsAnalytical Skills

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

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

Hard Skills

MS ProjectPlaniswareFTE ForecastingCritical Path VisualizationFinancial ReportingResource Demand ManagementScope ControlRisk ManagementTimeline ManagementGovernance Documentation

Soft Skills

Team LeadershipCommunication SkillsDecision-MakingMentoringPresentation Skills

Certifications & Qualifications

Bachelor's Degree

Industry Keywords

PharmaceuticalHealthcareClinical TrialsGlobal EnvironmentsMulti-Functional Teams

About the role

Key responsibilities & impact

Create, manage, and maintain integrated study schedules in MS Project, including Key Event Maps, Roadmaps, and critical path visualization aligned in Planisware
Assure Clinical timelines in Planisware align to MS Project schedules and coordinate integrated clinical plans with Clinical Development Team project plans
Ensure proper resource demand is reflected
Develop Planisware scenarios for budget, timeline, and FTE forecasting
Generate situational operational scenarios
Collect, consolidate, and report financial, timeline, and resource data for governance approvals and external funding partnerships
Manage scope control, FTE, and Out of Pocket variances
Document key decisions, actions, risks, issues, lessons learned, and trial governance documentation
Ensure risks are captured and monitored
Manage budgets effectively and adjust forecasts to reflect current thinking
Drive and facilitate after action review meetings and document results
Work with the team to assess and remediate impacts to scope, budget, and timelines
Support team-based reporting
Mentor and support onboarding of new team members, particularly those in Trial Management

Requirements

What you’ll need

Bachelor’s degree required
Minimum of 4 years in Pharmaceutical, Healthcare or related industries
Strong Project Management experience
Excellent leadership skills and proven ability to foster team productivity and cohesiveness
Experience leading without authority and in multi-functional matrixed and global environments
Excellent decision-making, analytical, and strong financial management skills
Strong communication and presentation skills
Up to 10% domestic and international travel
Preferred: Knowledge of Clinical Research Operations
Preferred: 2–3 years of experience managing multiple aspects of global clinical trial execution across Phases I–IV

Benefits

Comp & perks

Annual bonus with set target (% of pay) depending on pay grade / location
Vacation days
Parental leave for a minimum of 12 weeks
Bereavement leave
Caregiver leave
Volunteer leave
Well-being reimbursement
Programs for financial, physical and mental health
Service anniversary and recognition awards
Participation in several insurance plans for employees and eligible dependents in some locations
Netherlands annual base pay includes an 8% holiday allowance