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Emerald Clinical
Emerald Clinical
501 – 1000 Darbinieki
KonsultācijasLoģistikaVeselības aprūpe
Emerald Clinical ir globāla klīnisko pētījumu organizācija (CRO), kas dibināta Āzijas un Klusā okeāna reģionā. Aptuveni 25 gadus tā ir atbalstījusi biofarmācijas, medicīnas ierīču un diagnostikas uzņēmumus, nodrošinot pilna cikla klīnisko pētījumu pakalpojumus. Vairāk nekā 800 cilvēku komanda strādā vairāk nekā 40 vietās un vada pētījumus no agrīnās izstrādes līdz reģistrācijai un posmam pēc laišanas tirgū, tostarp klīniskās operācijas, projektu vadību un pētījumu personāla nodrošināšanu. Uzņēmums apvieno zinātnisko kompetenci un operatīvo atbalstu, lai veicinātu zāļu un medicīnas ierīču izstrādi.
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Vakances uzņēmumā

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.

SGSingapūraAttālinātiPilna slodzeVidējais līmenisVecākais speciālistsNepieciešamā Valoda: angļuLīgumu speciālistsVispārīgi
Google Cloud Platform

Apraksts

  • 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

Prasības

  • 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

Priekšrocības

  • 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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