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Innovaderm Research Inc.

Project Director, Early Phase and Translational Research – Europe

Innovaderm Research Inc.

Project Director overseeing multinational dermatology and rheumatology clinical trials for specialized CRO Indero. Managing portfolios, budgets, regulatory compliance, and Project Managers across Europe.

Posted 8/19/2026full-timeRemote • 🇪🇺 Anywhere in EuropeLeadWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates extensive expertise in clinical project management, overseeing large-scale clinical studies while ensuring compliance with regulatory requirements and quality standards. Proven ability to lead project teams, manage budgets, and drive operational efficiencies across therapeutic areas.

Highest-signal resume keywords
Clinical Project ManagementRegulatory ComplianceBudget ManagementTherapeutic Area ExpertiseMentoring and Coaching

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
Project ManagementFinancial TrackingProposal DevelopmentRisk MitigationPerformance ImprovementMultinational Trial ManagementVendor ManagementStudy DesignData AnalysisContingency Planning
Soft Skills
LeadershipCommunicationClient Relationship ManagementTeam BuildingProblem Solving
Tools & Technologies
Tracking ToolsAnalysis ToolsProject Management Software
Certifications & Qualifications
PMP CertificationPRINCE2 Certification
Industry Keywords
Good Clinical PracticesHealth Canada RegulationsFDA RegulationsDermatology TrialsRheumatology TrialsCRO ExperiencePhase III Clinical TrialsMulticentered StudiesOperational StrategyClient Presentations

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Oversee a portfolio or program of clinical studies and the Project Managers assigned to operationalize awarded studies
  • Ensure studies reflect therapeutic-area and client-specific requirements
  • Represent Indero to customers, maintain satisfaction levels, and communicate program deliverables
  • Ensure studies progress according to quality standards, SOPs, GCPs, regulatory requirements, and ICH guidelines
  • Oversee executed contracts and financial aspects, including study budgets and expenses
  • Maintain and evaluate project progress using timelines and tracking/analysis tools
  • Maintain in-depth therapeutic and/or client-specific knowledge for the assigned portfolio
  • Apply study-specific learning across assigned studies and clients
  • Lead contingency planning and risk-mitigation strategies
  • Lead operational input to proposal development and pricing, including operations strategy
  • Drive performance improvement, operational efficiencies, and innovative strategies
  • Provide line-management oversight and contribute to Project Management leadership as an operational and therapeutic-area expert

Requirements

What you’ll need
  • At least 15 years industry experience
  • Minimum of 5 years at a CRO
  • At least 10 years of clinical project management experience, including management of all project phases from start-up to closure, all functional services, and vendor management
  • Experience in dermatology or rheumatology trials is required
  • Experience with mid-size and large studies (>10–15 countries) in multiple regions (NA, SA, APAC, MENA, Europe) is desirable
  • Experience leading concurrent multicentered, multinational Phase III clinical trials, including project budget financial tracking and forecasting
  • Substantial experience in project supervision, mentoring, and coaching project managers
  • Substantial experience with business development tasks, including proposal development, client presentations, and bid defense meetings
  • Participation in mentoring and coaching of a representative number of project managers
  • Bachelor of Science in a relevant discipline
  • PMP or PRINCE2 Certification is an asset
  • Master's degree is an asset
  • Good knowledge of Good Clinical Practices and applicable Health Canada and FDA regulations/guidelines
  • Must be legally able to work in Europe

Benefits

Comp & perks
  • Flexible work schedule
  • Home-based position
  • Ongoing learning and development
  • Attractive advancement opportunities
  • Equitable treatment and equal opportunity
  • Accommodations throughout the recruitment and selection process for applicants with disabilities, upon request