Parexel
Parexel
Parexel este o organizație globală de cercetare clinică ce deservește companii biofarmaceutice pe parcursul dezvoltării de medicamente noi. Activitatea sa acoperă studii clinice de fază I–IV, gestionarea portofoliilor și a studiilor, strategia de reglementare, accesul la piață și planificarea ciclului de viață. Cu peste 21.000 de profesioniști, Parexel îmbină expertiza clinică, de reglementare și terapeutică cu perspectivele pacienților și designuri inovatoare ale studiilor. Compania sprijină cercetarea în domenii precum oncologia, neuroștiințele și bolile rare, punând accent pe eficientizarea dezvoltării clinice și pe orientarea acesteia către pacienți.

Site Care Partner I - Clinical Research (Israel Remote)

Serve as Parexel’s primary contact for investigator sites in Israel. Support clinical-trial start-up, monitoring, recruitment, quality, and patient safety throughout the study lifecycle.

Descriere

  • Represent the client to investigative sites throughout the study lifecycle
  • Provide site support and engagement, resolve issues, and protect the client’s reputation
  • Serve as the primary client contact for investigative sites
  • Manage site start-up activities through activation
  • Develop and maintain investigator-site relationships
  • Support sites from recommendation through study completion
  • Drive site-level recruitment and operational performance
  • Protect quality standards and patient safety at investigator sites
  • Support country and site selection activities under supervision
  • Work with stakeholders and provide local intelligence for country outreach surveys, investigator strategies, and client pipeline opportunities
  • Support sponsor clinical studies through Parexel FSP

Cerințe

  • A scientific or technical healthcare degree is preferred, together with extensive knowledge of clinical-trial methodology
  • BS, BSc, MS, MSc, or equivalent qualification plus five years of clinical research and/or quality-management experience
  • Professional fluency in English is required
  • Additional language skills are advantageous
  • At least eight years of site-management or clinical research associate monitoring experience
  • Experience reviewing reports
  • Oncology experience
  • Strong understanding of clinical-development processes, particularly monitoring
  • Experience overseeing third parties and/or working in quality assurance is preferred
  • Clinical-development project-management experience is preferred
  • Ability to lead, troubleshoot, and influence delivery
  • Experience implementing centrally designed initiatives locally
  • Knowledge of applicable country quality and regulatory requirements
  • Knowledge of country- or cluster-level site intelligence for site recommendations
  • Knowledge of clinical-trial methodology, drug development, monitoring, GCP, FDA, and country-specific regulatory environments
  • Experience with site activation and study start-up
  • Strong networking and relationship-building abilities
  • Ability to manage projects and cross-functional processes
  • Availability for regular travel within the country and region, typically three to five visits per month

Beneficii

  • Premium salary
  • Attractive benefits package
  • Car or company car
  • Health, dental, and vision medical plan
  • Life assurance
  • Positive work environment
  • Team-oriented and collaborative culture
  • Innovative technology
  • Comprehensive training
  • Long-term career development opportunities
  • Opportunities to take on greater responsibility or develop skills in other Parexel FSP departments

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