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Syneos Health
Syneos Health
H1B Visa SponsorConsultingHealthcareLogistics
Syneos Health is a fully integrated biopharmaceutical solutions organization that helps clients move therapies from clinical development to commercial delivery. Its teams combine clinical, medical affairs, commercial, technology, and market insights to address changing healthcare needs and support the development and launch of important treatments worldwide.
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Clinical Trial Coordinator, Single Sponsor — Germany Remote

Coordinate sponsor-site activities, regulatory documentation, clinical supplies, and study tracking for Syneos Health’s biopharmaceutical trials. Support site communications, meetings, audits, and corrective actions across assigned studies.

DEGermanyRemoteFull-timeMiddleSeniorEnglish RequiredClinical Trial CoordinatorGeneral
Google Cloud Platform

Description

  • Follow applicable corporate and clinical operations policies, standard operating procedures, and work instructions
  • Support Clinical Monitoring staff with site management and represent the sponsor at assigned study sites
  • Communicate with sites to confirm adherence to protocols, study procedures, and applicable guidelines
  • Create and maintain project files and manage related correspondence
  • Participate in file audits
  • Prepare and maintain site manuals, reference materials, and related documentation
  • Enter, update, and maintain clinical tracking data in relevant databases
  • Monitor incoming and outgoing clinical and regulatory documents and updates
  • Manage the shared mailbox, respond to site requests, and route correspondence appropriately
  • Coordinate the ordering, packaging, shipment, and tracking of site supplies and materials
  • Support team meeting logistics, attend meetings, and prepare minutes and action items
  • Identify and address potential issues while implementing corrective actions
  • Complete required clinical research training
  • Provide training or mentorship to junior Clinical Operations Specialists when needed

Requirements

  • An associate degree is preferred, or an equivalent qualification
  • Relevant clinical research, pharmaceutical, biotechnology, or related experience may substitute for a degree
  • Working knowledge of medical terminology, clinical data, and ICH/GCP is preferred
  • Ability to prioritize effectively while managing multiple tasks
  • Strong attention to detail, accuracy, and organizational capability
  • Excellent communication, presentation, and interpersonal skills
  • Willingness and ability to adopt new technologies
  • Up to 10% travel may be required

Benefits

  • Career development and advancement opportunities
  • Supportive, engaged line management
  • Technical and therapeutic-area training
  • Peer recognition programs
  • Total rewards program
  • Total Self culture
  • Diversity, inclusion, and belonging initiatives

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