Syneos Health
Syneos Health
Syneos Health mijozlarga davolash usullarini klinik ishlab chiqish bosqichidan tijoriy foydalanishga qadar yetkazishga yordam beradigan, biofarmatsevtik yechimlarni to‘liq integratsiyalashgan tarzda taqdim etuvchi tashkilotdir. Uning jamoalari klinik tadqiqotlar, tibbiy faoliyat, tijoriy yo‘nalish, texnologiya va bozor haqidagi ma’lumotlarni birlashtirib, sog‘liqni saqlash sohasining o‘zgarib borayotgan ehtiyojlarini qondiradi hamda butun dunyoda muhim davolash usullarini ishlab chiqish va bozorga chiqarishni qo‘llab-quvvatlaydi.

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.

Tavsif

  • 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

Talablar

  • 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

Imtiyozlar

  • 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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