Netherlands
17 Aug 2026
Project Manager (CTL) - Sponsor dedicated logo

Project Manager (CTL) - Sponsor dedicated

Syneos Health

Project Manager (CTL) - Sponsor dedicated

Syneos Health is seeking a Project Manager (Clinical Trial Lead) to join a global team based in the Netherlands, dedicated to a single sponsor partnership. The role involves leading interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements, and managing project delivery, budgets, and client relationships. Requires a Bachelor's degree in life sciences or related field, strong CRO and therapeutic experience, and willingness to travel approximately 25%.

On-siteFull-timeEntry LevelClinical ResearchGood Clinical Practice

Salary

Not specified

Work Location

Netherlands, NL

Work Model

On-site

Employment Type

Full-time

Experience Level

Not Applicable

Core Qualifications

Technical (Must-have)
Clinical researchGood Clinical PracticeICH guidelinesRegulatory requirementsProject managementBudget managementTime managementTherapeutic area expertiseTMFDatabasesInspection readinessRisk mitigationContingency planningClinical monitoring
Soft Skills
Organizational skillsCommunicationPresentationInterpersonal skillsIndependent workAdaptability to new technologiesRelationship building

Key Responsibilities

  • Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP’s, and regulatory requirements.
  • Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer’s and the Company’s contractual agreement.
  • Lead project team to ensure quality, timelines and budget management.
  • Accountable for the financial performance of each project. Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.
  • Ensure studies are conducted in compliance with GCP, relevant SOP’s and regulatory requirements. Accountable for all project deliverables for each project assigned.
  • Responsible for quality and completeness of TMF for assigned projects.
  • Accountable for maintenance of study information on a variety of databases and systems.
  • Responsible for study management components of inspection readiness for all aspects of the study conduct. Oversight for development and implementation of project plans.
  • Plan, coordinate and present at internal and external meetings. Prepare project management reports for clients and management.
  • Developing contingency planning and risk mitigation strategies to ensure successful delivery of study goals.
  • Develops strong relationships with current clients to generate new and/or add-on business for the future.
  • May participate in bid defense meetings where presented as potential project manager.
  • May be required to line manage other project management team members and clinical monitoring staff.
Project ManagerClinical Trial LeadBiotechnology ResearchLife SciencesCROGCPOn-siteFull-timeNetherlandsSponsor dedicated