1 week ago

Clinical Operation Specialist

Syneos Health

Amsterdam

1 week ago

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Clinical Operation Specialist position at Syneos Health, a leading life sciences services organization. The role involves coordinating clinical trials, managing study documentation, and supporting site management activities. Requires a Master's degree in biomedical sciences, fluency in Dutch, and willingness to work from Haarlem office.

HybridFull-timeEntry LevelClinical ResearchTrial Master File (TMF)

Clinical Operation Specialist

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HybridFull-timeEntry LevelClinical Research

Salary

Not specified

Work Location

Amsterdam, North Holland, Netherlands, NL

Work Model

Remote, but willing to work from Haarlem office on a regular basis

Employment Type

Full-time

Experience Level

Established and experienced support individual contributor

Core Qualifications

Technical (Must-have)

Clinical ResearchTrial Master File (TMF)Regulatory DocumentsDatabase ManagementCommunicationInterpersonal Skills

Soft Skills

CommunicationInterpersonal SkillsAdaptabilityTeam CollaborationProblem Solving

Key Responsibilities

•Perform activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions
•Assist Clinical Monitoring staff with site management activities
•Create and assist with maintenance of Trial Master File (TMF) and project files
•Prepare and maintain site manuals, reference tools and other documents
•Maintain, update, and input clinical tracking information into databases
•Track incoming and outgoing clinical and regulatory documents
•Manage shared mailbox, process site requests and route correspondence
•Coordinate ordering, packaging, shipping and tracking of site supplies and materials
•Assist with coordination of team meetings and prepare meeting minutes
•Handle receipt, tracking and disposition of Case Report Forms and Queries

Clinical ResearchClinical Trial CoordinatorBiotechnologyPharmaceuticalNetherlandsFull-timeRemoteHybridEntry Level

Key Responsibilities

•Perform activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions

•Assist Clinical Monitoring staff with site management activities

•Create and assist with maintenance of Trial Master File (TMF) and project files

•Prepare and maintain site manuals, reference tools and other documents

•Maintain, update, and input clinical tracking information into databases

•Track incoming and outgoing clinical and regulatory documents

•Manage shared mailbox, process site requests and route correspondence

•Coordinate ordering, packaging, shipping and tracking of site supplies and materials

•Assist with coordination of team meetings and prepare meeting minutes

•Handle receipt, tracking and disposition of Case Report Forms and Queries