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Clario
Clario
5 001 – 10 000 Xodimlar
H1B vizasi homiysiKonsaltingLogistikaSog‘liqni saqlash
Clario tadqiqotni boshlashdan tortib uni amalga oshirishgacha bo‘lgan klinik sinovlarni qo‘llab-quvvatlaydigan texnologiyalar va xizmatlarni ishlab chiqadi. Kompaniyaning klinik sinovlarni boshqarish platformasi onkologiya, kardiologiya va nevrologiya kabi terapevtik yo‘nalishlarda elektron klinik natijalarni baholash, yurak xavfsizligi, tibbiy tasvirlash, aniq harakat va nafas olishni monitoring qilish yechimlarini birlashtiradi. Clario, shuningdek, yakuniy ko‘rsatkichlarni tahlil qilishda sun’iy intellektdan foydalanib, tadqiqot guruhlariga bemorlarning maxfiyligi va xavfsizligini ta’minlagan holda izchil sinov ma’lumotlarini to‘plashda yordam beradi. Kompaniya markazlashtirilmagan va gibrid tadqiqot modellarida ishlaydi hamda global mamlakatlar tarmog‘idagi klinik tadqiqot dasturlariga xizmat ko‘rsatadi. Clario’dagi karyera sog‘liqni saqlash texnologiyalari, klinik ma’lumotlar operatsiyalari va dori vositalari tadqiqotlarida ishlatiladigan vositalarni ishlab chiqishga hissa qo‘shish imkonini beradi.
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Kompaniyadagi ish o‘rinlari

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.

USAmerika Qo‘shma ShtatlariMasofaviyTo‘liq stavkaSeniorTalab Qilinadigan Til: inglizchaKlinik operatsiyalar
Google Cloud Platform

Tavsif

  • 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.

Talablar

  • 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.

O‘xshash ish o‘rinlari

AstraZeneca

Senior Digital Business Process and Product Lead

AstraZeneca
H1B vizasi homiysiBiotexnologiyaFarmatsevtika mahsulotlariSog‘liqni saqlash
USAmerika Qo‘shma ShtatlariMDMerilend
124 000 $ – 185 000 $ / yil
OfisdaTo‘liq stavkaSeniorTalab Qilinadigan Til: inglizchaBiznes operatsiyalari
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Ishlab chiqarishKonsaltingLogistika
GBBuyuk BritaniyaOfisdaTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaMijozlarni qo‘llab-quvvatlash
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Newstel Worldwide

Part-Time Danish-Speaking Customer Service Agent (Portugal, Remote)

Newstel Worldwide
201 – 500 Xodimlar
KonsaltingLogistikaMarketing
PTPortugaliya
11 € – 14 € / soat
MasofaviyYarim stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: danTalab Qilinadigan Til: inglizchaMijozlarni qo‘llab-quvvatlash

Provide remote customer support in Danish for Newstel’s multilingual BPO customers while meeting service and quality targets. This part-time role covers email, chat and phone enquiries from Portugal.

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