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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

Clinical Lead / Clinical Trial Manager – Remote, United States

Lead global clinical trial delivery for Emerald Clinical, coordinating sites, timelines, budgets, compliance, and cross-functional execution from start-up through close-out.

USStatele Unite ale Americii
130.000 $ – 160.000 $ / an
RemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • Direct clinical trials through start-up and close-out
  • Lead site selection and feasibility work with CRAs and investigators
  • Control study timelines, budgets, and delivery commitments
  • Oversee protocol administration, site initiation, monitoring, and overall study progress
  • Coordinate with sponsors, investigators, internal stakeholders, and project teams
  • Maintain compliance with GCP, FDA regulations, and company SOPs
  • Coach and develop CRAs and site staff
  • Safeguard protocol adherence and data integrity

Cerințe

  • Experience in renal studies
  • Bachelor’s degree in a science-related discipline, with an RN preferred, plus industry experience
  • One to two years of experience as a Clinical Trial Manager or Clinical Lead
  • Substantial experience in clinical monitoring and site management
  • Experience in oncology or other complex indications is preferred
  • CCRA or CCRP certification is strongly preferred
  • Advanced knowledge of GCP, FDA regulations, and clinical trial best practices
  • Proven ability to coordinate multiple projects, timelines, and stakeholders efficiently
  • Strong leadership, problem-solving, and communication capabilities
  • Availability to travel up to 20% as needed

Beneficii

  • Competitive pay with a salary and benefits package tailored to the role
  • Hybrid or remote work options based on location and role
  • Professional development opportunities and access to a worldwide network of scientific leaders
  • Wellbeing programs that promote work-life balance, health, and team connection
  • Participation in global employee engagement surveys
  • Employee recognition initiatives
  • Team-building activities
  • Work across varied international projects and client engagements

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