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Emerald Clinical
Emerald Clinical
501 – 1.000 Angajați
Asistență medicalăConsultanțăLogistică
Emerald Clinical este o organizație globală de cercetare clinică (CRO), fondată în regiunea Asia-Pacific. De aproximativ 25 de ani, sprijină companii din domeniul biofarmaceutic, al dispozitivelor medicale și al diagnosticării prin servicii complete pentru studii clinice. Echipa sa, formată din peste 800 de persoane, lucrează în mai mult de 40 de locații și gestionează studii începând din primele etape de dezvoltare până la autorizare și perioada de după lansare, inclusiv operațiuni clinice, management de proiect și asigurarea personalului pentru studii. Activitatea companiei îmbină expertiza științifică și sprijinul operațional pentru a contribui la dezvoltarea medicamentelor și dispozitivelor medicale.
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Locurile de muncă ale companiei

Site Contracts Specialist – Singapore (Remote)

Manage clinical trial agreements and site budgets for Emerald Clinical Trials. Support global study start-up, contract negotiations, compliance, and site activation.

SGSingaporeRemoteNormă întreagăNivel mediuSeniorLimbă Obligatorie: englezăGeneralSpecialist contracte
Google Cloud Platform

Descriere

  • Prepare, review, negotiate, and manage clinical trial agreements, amendments, and related contract documents
  • Develop, negotiate, and oversee site budgets within approved sponsor parameters
  • Coordinate contract and budget activities among sponsors, investigative sites, legal teams, and internal stakeholders
  • Deliver contract and budget execution against agreed study timelines and project milestones
  • Maintain contract management systems, trackers, templates, and supporting records
  • Check contractual documents for accuracy, completeness, regulatory compliance, sponsor requirements, and company policies
  • Track contract progress and address negotiation barriers
  • Support site payments and coordinate accurate, timely invoicing
  • Assist with country and site start-up, document collection, and ongoing study maintenance
  • Organize and maintain contract records throughout the study lifecycle
  • Attend project meetings and report contract and budget progress
  • Support quality programs, audits, inspections, and process improvement initiatives
  • Help develop systems, tools, and best practices for contract and budget administration

Cerințe

  • Bachelor’s degree or equivalent qualification in a scientific, healthcare, legal, business, or related field
  • Prior experience in a CRO, pharmaceutical company, or clinical research setting
  • Demonstrated experience negotiating site contracts and managing clinical trial budgets
  • Strong knowledge of clinical research workflows, study start-up, and site activation requirements
  • Working knowledge of ICH-GCP guidelines and relevant regulatory requirements
  • Excellent negotiation, communication, and stakeholder management abilities
  • Ability to assess and interpret contractual, legal, financial, and operational documents
  • Exceptional attention to detail, organization, and project coordination skills
  • Experience working across multiple countries and cultures is highly desirable
  • Proficiency with contract management systems, CTMS platforms, and Microsoft Office applications
  • Ability to work independently and collaborate effectively with cross-functional teams
  • Proactive, solutions-oriented approach to managing competing priorities in a fast-paced environment

Beneficii

  • Competitive salary and benefits package based on skills and experience
  • Remote or hybrid work options depending on location and business needs
  • Learning opportunities, mentorship, and access to global career pathways
  • Employee wellbeing programs supporting work-life balance, health, and engagement
  • Opportunity to contribute to international studies for leading sponsors across varied therapeutic areas
  • Collaborative workplace where expertise and contributions are recognized and valued

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