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Parexel
Parexel
H1B vīzas sponsorsKonsultācijasLoģistikaVeselības aprūpe
Parexel ir globāla klīnisko pētījumu organizācija, kas apkalpo biofarmācijas uzņēmumus visā jaunu zāļu izstrādes procesā. Tās darbība aptver I–IV fāzes klīniskos pētījumus, portfeļa un pētījumu pārvaldību, regulatīvo stratēģiju, piekļuvi tirgum un zāļu dzīves cikla plānošanu. Ar vairāk nekā 21 000 profesionāļu Parexel apvieno klīnisko, regulatīvo un terapeitisko jomu zināšanas ar pacientu ieskatiem un inovatīviem pētījumu plāniem. Uzņēmums atbalsta pētniecību tādās jomās kā onkoloģija, neirozinātne un retās slimības, koncentrējoties uz efektīvāku un pacientcentrētāku klīnisko izstrādi.
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Vakances uzņēmumā

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.

ILIzraēlaAttālinātiPilna slodzeVecākais speciālistsVadošais speciālistsNepieciešamā Valoda: angļuPartnerprogrammu vadītājsPartneru mārketings
Google Cloud Platform

Apraksts

  • 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

Prasības

  • 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

Priekšrocības

  • 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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