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Alcedis - a HUMA company
Alcedis - a HUMA company
51 – 200 Xodimlar
KonsaltingLogistikaSog‘liqni saqlash
Alcedis - a HUMA company biotexnologiya va farmatsevtika sohalaridagi ishlanmalar uchun texnologiyalar asosida olib boriladigan klinik tadqiqotlarga ixtisoslashgan shartnoma asosidagi tadqiqot tashkilotidir. Uning jamoasi klinik operatsiyalarni loyihalarni boshqarish, ma’lumotlarni boshqarish, monitoring, tartibga solish masalalari, biostatistika, tibbiy matnlar yozish va farmakonazorat yo‘nalishlari bilan birlashtiradi. Alcedis, shuningdek, moslashuvchan elektron holat hisobotlari shakllari, mobil ilovalar, integratsiyalar, ma’lumotlar fani va sun’iy intellekt imkoniyatlarini o‘z ichiga olgan raqamli tadqiqot vositalarini ishlab chiqadi hamda tadqiqotlarni dastlabki ishlab chiqish bosqichidan tartibga soluvchi organlar tomonidan tasdiqlanishi va real hayotdagi dalillarni to‘plashgacha qo‘llab-quvvatlaydi.
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Kompaniyadagi ish o‘rinlari

Clinical Project Manager – Clinical Research and IT

Manage U.S. clinical research projects and digital trial technologies for Alcedis, a contract research organization. Responsibilities include regulatory submissions, budgets, site coordination, technology oversight, and collaboration with international teams.

USAmerika Qo‘shma Shtatlari
80 000 $ – 110 000 $ / yil
MasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaKlinik operatsiyalar

Tavsif

  • Direct clinical trial planning and delivery from study start-up through ongoing management
  • Maintain essential study records and documentation, including TMF and ISF
  • Track milestones and keep study execution aligned with the approved Project Plan and objectives
  • Manage project budgets, financial controls, and reporting to the functional unit head
  • Prepare and oversee submissions to the FDA, IRBs, and other applicable authorities, including INDs, CTAs, amendments, and safety reports
  • Coordinate cross-functional project teams working across the United States and Germany
  • Oversee the work and deliverables of subcontractors
  • Manage clinical trial technologies and digital platforms such as ePRO, eCOA, and eCRF
  • Help manage supporting IT services and verify that solutions meet the needs of U.S. clients and participants
  • Work with technical teams to troubleshoot issues, deploy updates, and improve workflows
  • Create and implement processes, SOPs, work instructions, and standardized records
  • Coordinate trial sites through communication, training, document shipment and tracking, and payment processing
  • Travel may be required for project-related activities

Talablar

  • Bachelor’s degree in natural sciences, a related discipline, or an equivalent qualification; an advanced degree is preferred
  • 3–5+ years of experience working as a Clinical Project Manager in clinical research
  • Previous experience in a contract research organization is required
  • Demonstrated ability to independently manage and complete IRB or ethics committee submissions
  • Working knowledge of data privacy, data protection, and clinical research standards, including The Belmont Report, HIPAA, and FDA 21 CFR Part 11
  • Knowledge of GDPR is an advantage
  • Comfort working independently with limited structure and without local colleagues or on-site management
  • Experience using electronic data systems and databases
  • Strong working knowledge of Microsoft Office
  • Ability to work confidently with clinical research technology and digital platforms
  • Strong interpersonal, communication, and organizational capabilities
  • Effective collaborator across functions, teams, and international boundaries
  • Fluent written and spoken English
  • Must reside in the Eastern or Central United States

Imtiyozlar

  • 15 days of paid vacation annually
  • 6 paid sick days annually
  • Health, dental, and vision coverage for employees and dependents
  • Employer-provided life insurance
  • Health Savings Account (HSA)
  • 401(k) plan without an employer match
  • Growth-focused workplace oriented toward the future
  • Challenging projects designed to have meaningful impact
  • Open, collaborative culture supported by a flat organizational structure
  • Dedicated and supportive team environment
  • Varied responsibilities with autonomy over project ownership
  • Flexible hours that support work-life balance

O‘xshash ish o‘rinlari

Sikla GmbH

Customer and Sales Support Specialist

Sikla GmbH
501 – 1 000 Xodimlar
Ishlab chiqarishKonsaltingLogistika
GBBuyuk BritaniyaOfisdaTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaMijozlarni qo‘llab-quvvatlash
ERP

Support Sikla UK’s technical modular support systems business in Milton Keynes, handling customer and sales enquiries from quotation through delivery. Coordinate orders, documentation, logistics, and ERP administration with customers and internal teams.

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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.

Ochish