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Emerald Clinical
Emerald Clinical
501 – 1 000 Darbuotojai
KonsultavimasLogistikaSveikatos priežiūra
„Emerald Clinical“ yra pasaulinė klinikinių tyrimų organizacija (CRO), įkurta Azijos ir Ramiojo vandenyno regione. Maždaug 25 metus ji teikia visapusiškas klinikinių tyrimų paslaugas biofarmacijos, medicinos prietaisų ir diagnostikos įmonėms. Daugiau kaip 800 darbuotojų komanda dirba daugiau nei 40 vietų ir valdo tyrimus nuo ankstyvojo kūrimo etapo iki registracijos bei laikotarpio po pateikimo į rinką, įskaitant klinikines operacijas, projektų valdymą ir tyrimų personalo komplektavimą. Įmonė derina mokslinę kompetenciją ir veiklos palaikymą, kad padėtų plėtoti vaistus ir medicinos prietaisus.
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Darbai įmonėje

Clinical Trial Specialist, APAC (Mandarin Speaking)

Support Emerald Clinical’s global early-phase trials across APAC. Coordinate study records, meetings, budgets, vendors, and trial master file activities.

TWTaivanasHibridinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųPrivaloma Kalba: kinųKlinikiniai tyrimai
Google Cloud Platform

Aprašymas

  • Provide daily operational and administrative assistance to Early Phase Project Managers
  • Help coordinate and deliver global clinical trials
  • Manage study records and keep project trackers and systems current
  • Arrange internal and external project meetings, including schedules, agendas, and minutes
  • Track action items and deliverables with cross-functional teams and vendors
  • Assist communications among clinical sites, vendors, and internal teams
  • Support study start-up, ongoing management, and close-out
  • Follow SOPs, ICH-GCP guidelines, and applicable regulatory standards
  • Coordinate meetings with clients, internal teams, and vendors
  • Draft minutes for internal and external stakeholders
  • Assist with study and site budgets, including tracking payments
  • Maintain trial master file records, upload documents, perform quality checks, and conduct regular reviews for assigned projects

Reikalavimai

  • Fluent Mandarin
  • Bachelor’s degree in life sciences, pharmacy, nursing, or a related discipline
  • Two to three years of clinical research experience, particularly in trial coordination and project support
  • Experience supporting clinical trials at a CRO, sponsor, or similar organization
  • Understanding of clinical trial phases or experience supporting studies from start to finish
  • Familiarity with trial documentation, processes, and regulations, including ICH-GCP
  • Comfort using Microsoft Office and clinical systems such as CTMS and eTMF
  • Strong organization skills and ability to prioritize and manage multiple tasks
  • Excellent written and spoken communication skills
  • Proactive, detail-focused, collaborative approach
  • Proficiency in Word, Excel, and PowerPoint
  • MS Project knowledge is an advantage and can be learned
  • Experience or solid knowledge of project management systems, including CTMS and financial or resource planning systems
  • Experience maintaining TMFs, uploading documents, conducting quality checks, and performing regular reviews
  • Ability to assist with study and site budgets, including investigator site and vendor payments and payment tracking

Privalumai

  • Purpose-led work supporting clinical trials in renal, cardiometabolic, and oncology therapies
  • Hybrid or remote work arrangements, depending on location and role
  • Opportunities for career development and learning
  • Access to an international network of scientific leaders
  • Wellbeing programs that support work-life balance, health, and team connection
  • Global employee engagement surveys
  • Employee recognition programs
  • Team-building activities
  • Experience with varied international projects and clients
  • Competitive pay and a benefits package tailored to the role

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