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Emerald Clinical
Emerald Clinical
501 – 1000 Zaposleni
LogistikaSvetovanjeZdravstveno varstvo
Emerald Clinical je globalna organizacija za klinične raziskave (CRO), ustanovljena v azijsko-pacifiški regiji. Približno 25 let podpira biofarmacevtska podjetja, proizvajalce medicinskih pripomočkov in diagnostična podjetja z vsemi storitvami, potrebnimi za klinična preskušanja. Njena ekipa z več kot 800 člani deluje na več kot 40 lokacijah in vodi študije od zgodnjih faz razvoja do registracije ter obdobja po prihodu izdelka na trg, vključno s kliničnimi operacijami, vodenjem projektov in zagotavljanjem osebja za preskušanja. Podjetje združuje znanstveno strokovno znanje in operativno podporo za pospeševanje razvoja zdravil in medicinskih pripomočkov.
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Delovna mesta v podjetju

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.

TWTajvanHibridnoPolni delovni časJuniorSrednja ravenZahtevani Jezik: angleščinaZahtevani Jezik: kitajščinaKlinične raziskave
Google Cloud Platform

Opis

  • 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

Zahteve

  • 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

Ugodnosti

  • 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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