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Clario
Clario
5001 – 10 000 Darbinieki
H1B vīzas sponsorsKonsultācijasLoģistikaVeselības aprūpe
Clario izstrādā tehnoloģijas un pakalpojumus, kas atbalsta klīniskos pētījumus no pētījuma uzsākšanas līdz tā īstenošanai. Uzņēmuma klīnisko pētījumu pārvaldības platforma apvieno risinājumus elektroniskai klīnisko iznākumu novērtēšanai, sirds drošības uzraudzībai, medicīniskajai attēlveidošanai, precīzai kustību uzraudzībai un elpošanas monitoringam tādās terapeitiskajās jomās kā onkoloģija, kardioloģija un neiroloģija. Clario izmanto mākslīgo intelektu arī iznākumu analīzē, palīdzot pētniecības komandām vākt konsekventus pētījumu datus, vienlaikus atbalstot pacientu privātumu un drošību. Uzņēmums strādā ar decentralizētiem un hibrīdiem pētījumu modeļiem un apkalpo klīniskās pētniecības programmas globālā valstu tīklā. Darbs Clario sniedz iespēju dot ieguldījumu veselības aprūpes tehnoloģiju, klīnisko datu operāciju un zāļu pētniecībā izmantotu rīku izstrādē.
LinkedIn
Vakances uzņēmumā

Senior Lead Clinical Project Manager

Lead global clinical research studies at Clario, part of Thermo Fisher Scientific, overseeing delivery, teams, compliance, risk, and operational performance.

USAmerikas Savienotās ValstisAttālinātiPilna slodzeVecākais speciālistsNepieciešamā Valoda: angļuKlīniskās operācijas
Google Cloud Platform

Apraksts

  • Oversee global clinical study management and project delivery.
  • Assess study progress, resource needs, and team workloads, then implement adjustments and mitigation plans.
  • Identify, assess, and reduce risks across assigned studies and programs.
  • Handle escalations and resolve operational, client, and project issues.
  • Help Clinical Project Managers communicate study status, risks, timelines, and deliverables to clients.
  • Coordinate collaboration among internal and external stakeholders across functions.
  • Organize and lead regular project status meetings.
  • Manage assigned studies from start-up through execution and closeout.
  • Guide study teams across therapeutic areas and programs.
  • Work with senior leaders to prioritize deliverables, address resource needs, and share critical project updates.
  • Improve operations through ongoing process improvement initiatives.
  • Lead departmental initiatives from planning through execution, communication, training, and progress reporting.
  • Lead therapeutic area or imaging operational readiness and implement new processes and procedures.
  • Track operational challenges and recommend ways to improve study delivery, quality, and efficiency.
  • Coach, mentor, and develop project management team members.
  • Help onboard and train new team members.
  • Allocate team assignments and distribute workloads.
  • Set and uphold departmental standards, SOP compliance, and study management practices.
  • Review and revise project management and therapeutic team procedures.
  • Take on other duties, assignments, and special projects as needed.

Prasības

  • Bachelor's degree in life sciences, pharmacy, nursing, or a related field; a master's degree is preferred.
  • 5–10 years of clinical research experience in a CRO, pharmaceutical, biotechnology, or related clinical development setting, including substantial project management responsibility.
  • Prior people management and leadership experience in clinical development, clinical operations, or clinical trial management.
  • Strong understanding of clinical trial processes, project management methods, and drug development practices.
  • Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and FDA regulations.
  • Experience supporting global clinical studies and leading cross-functional teams across locations.
  • Medical imaging experience is preferred.
  • Demonstrated ability to coach, mentor, and develop team members.
  • Strong organization, prioritization, problem-solving, and decision-making skills.
  • Excellent written and verbal communication, including the ability to communicate effectively in English with internal and external stakeholders.
  • Proficiency with Microsoft Office and project management tools.
  • Attention to detail and the ability to manage competing priorities and adapt to changing business needs.
  • Valid passport and ability to travel up to 20% as needed.

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Veselības apdrošināšanaVeselības aprūpe
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H1B vīzas sponsorsFarmaceitiskie produktiVeselības apdrošināšanaVeselības aprūpe
SGSingapūraHibrīdiPilna slodzeVadošais speciālistsNepieciešamā Valoda: angļuKlientu atbalsts

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