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Fortrea

Clinical Research Manager – Sponsor Dedicated

Fortrea

. Lead and oversee local clinical trial operations .

Posted 10/23/2026full-timeLeiden • NetherlandsMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in leading clinical trial operations, ensuring regulatory compliance, and managing budgets and resources. Proficient in mentoring teams and fostering relationships with stakeholders to drive trial success.

Highest-signal resume keywords
Clinical Research ExperienceICH-GCP KnowledgeRegulatory ComplianceLeadership SkillsFluent in English and Dutch

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 Trial OperationsProtocol ComplianceSite SelectionVendor ManagementBudget OversightResource ForecastingMonitoring ExperiencePharmacovigilanceMedical AffairsCross-Functional Team Leadership
Soft Skills
Excellent CommunicationOrganizational SkillsTeam Performance MentoringIndependent WorkVirtual Environment Adaptability
Certifications & Qualifications
Master’s Degree in Life Sciences
Industry Keywords
PharmaCROHealthcareClinical Trial ProcessesLocal Regulations

About the role

Key responsibilities & impact
  • Lead and oversee local clinical trial operations
  • Ensure regulatory and financial compliance across protocols
  • Drive performance across assigned studies
  • Serve as the primary point of contact for investigators, vendors, and internal teams
  • Represent the client and build relationships supporting trial success
  • Ensure protocol compliance and performance
  • Monitor site activities, review reports, and address training needs
  • Oversee budgets, contracts, and resource forecasting
  • Align with regulatory, pharmacovigilance, medical affairs, and global teams

Requirements

What you’ll need
  • Master’s degree in life sciences or related field (or equivalent experience)
  • 6–8 years of clinical research experience in pharma, CRO, or healthcare
  • Previous monitoring experience is needed
  • Strong knowledge of ICH-GCP, local regulations, and clinical trial processes
  • Excellent communication, organizational, and leadership skills
  • Ability to manage multiple protocols and lead cross-functional teams
  • Fluent in English and Dutch (written and spoken)
  • Experience with site selection, start-up, and vendor management
  • Proven ability to mentor junior staff and foster team performance
  • Comfortable working independently and in virtual environments