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Thermo Fisher Scientific
Thermo Fisher Scientific
H1B vizos rėmėjasGamybaLogistikaSveikatos priežiūra
„Thermo Fisher Scientific“ kuria ir tiekia technologijas, laboratorijų produktus bei farmacijos paslaugas, padedančias vykdyti mokslinius tyrimus ir teikti sveikatos priežiūrą. Įmonės veikla apima gyvybės mokslų tyrimus, analitinių problemų sprendimą, laboratorijų našumo didinimą, diagnostiką, taip pat gydymo metodų kūrimą ir gamybą. Klientams visame pasaulyje ji teikia paslaugas pasitelkdama tarptautinę komandą ir prekių ženklų portfelį, kurį sudaro „Thermo Scientific“, „Applied Biosystems“, „Invitrogen“, „Fisher Scientific“, „Unity Lab Services“, „Patheon“ ir „PPD“. Įmonės karjeros galimybės apima su šiais pasiūlymais susijusias mokslo, sveikatos priežiūros, gamybos, logistikos ir paslaugų veiklas.
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Darbai įmonėje

Clinical Trial Coordinator, Peru (Remote)

Coordinate clinical trial start-up, feasibility, regulatory submissions, documentation, and site communications for a global clinical research organization. Maintain clinical systems, investigator files, study metrics, and related trial records.

PEPeruNuotolinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųBendraKlinikinių tyrimų koordinatorius

Aprašymas

  • Coordinate assigned clinical trial activities in line with task matrices.
  • Review departmental, internal, country, and investigator files and document findings.
  • Complete assigned work on schedule, within budget, and to required quality standards.
  • Support Activate, eTMF, and other clinical trial systems while keeping databases current.
  • Process client eTMF documents, conduct reviews, distribute communications, and prepare reports.
  • Analyze and reconcile study metrics and findings reports and help resolve site-documentation issues.
  • Coordinate Investigator Site File, Pharmacy binder, and non-clinical study supply materials.
  • Support study-specific translation materials and perform translation quality checks.
  • Keep current with SOPs, client instructions, and applicable regulatory requirements.
  • Conduct on-site feasibility visits in Asia Pacific when applicable.
  • Help schedule client and internal meetings and track local regulatory documents.
  • Support risk-based monitoring activities, study documentation, training, system access, and activity plans.
  • Transmit documents to the client and centralized IRB or IEC.
  • Maintain vendor trackers and assist with regulatory submissions.
  • Work with sites to obtain documents required for site selection.
  • Prepare regulatory compliance review packages with the project team.
  • Coordinate internal teams to keep site start-up aligned with the activation critical path.
  • Complete Site Interest Plans in CTMS and collect related documents when required.
  • Record communications, follow-ups, and survey responses in real time.
  • Review survey data for logical, complete, and relevant responses.
  • Work with teammates and clinical personnel on deadlines, site issues, and risks.
  • Maintain site-contact and follow-up plans and escalate concerns or non-compliance.
  • Apply local knowledge of site capacity and experience to recommend additional sites.
  • Work with Global Investigator Services to resolve investigator questions and maintain account and contact details.
  • Contribute to global feasibility strategy and process improvements.
  • Train new personnel on relevant processes and systems.
  • Use local market knowledge to identify and develop new clinical trial sites.

Reikalavimai

  • High school or secondary school diploma, or equivalent, plus relevant formal academic or vocational training.
  • A bachelor's degree is preferred.
  • Relevant experience equivalent to approximately 0–1 year of required job knowledge, skills, and abilities.
  • Equivalent combinations of appropriate education, training, and directly related experience may be considered.
  • Ability to work independently and collaboratively.
  • Strong organization and attention to detail.
  • Ability to analyze project-specific data and systems accurately and efficiently.
  • Strong customer focus and flexibility to reprioritize work.
  • Working knowledge of applicable country regulations, ICH Good Clinical Practice, organizational or client SOPs, and WPDs.
  • Strong English language and grammar skills, plus local-language proficiency when required.
  • Proficiency with Microsoft Word, Excel, and PowerPoint.
  • Ability to learn and use clinical trial database systems.
  • Ability to complete the organization's clinical training program.
  • Effective oral and written communication, interpersonal, negotiation, judgment, decision-making, risk management, and escalation skills.
  • Ability to follow project work instructions accurately.

Privalumai

  • Fully remote work arrangement.
  • Standard Monday–Friday schedule.
  • Occasional travel may be required.
  • Training and onboarding support.
  • Opportunity to buddy with and train new staff.

Susiję darbai

Knowtion Health

Remote Talent Acquisition Manager

Knowtion Health
501 – 1 000 Darbuotojai
H1B vizos rėmėjasDraudimasKonsultavimasLogistika
USJungtinės ValstijosALAlabamaAZArizonaFLFloridaIDAidahasKSKanzasasMEMeinasMIMičiganasMSMisisipėMOMisūrisNMNaujoji MeksikaNCŠiaurės KarolinaOKOklahomaPAPensilvanijaSCPietų KarolinaTNTenesisTXTeksasasVAVirdžinijaWVVakarų VirdžinijaWIViskonsinasNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųĮdarbinimas

Oversee recruiting systems, requisitions, analytics, and contingent workforce operations at Knowtion Health. Help support scalable hiring processes for a growing healthcare company.

Atidaryti
Napco National

Purchasing Coordinator, Saudi Arabia (Remote)

Napco National
5 001 – 10 000 Darbuotojai
LogistikaMaistas ir gėrimaiSveikatos priežiūra
SASaudo ArabijaNuotolinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųPirkimai

Coordinate purchasing operations for a manufacturing business in Saudi Arabia, from purchase orders and supplier deliveries to customs paperwork and material transfers. Support shipment clearance, invoice processing, supplier claims, and product certificate renewals.

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Terumo Medical Corporation

Region Manager, Terumo Interventional Systems Sales

Terumo Medical Corporation
1 001 – 5 000 Darbuotojai
H1B vizos rėmėjasGamybaKonsultavimasSveikatos priežiūra
USJungtinės ValstijosNJNaujasis Džersis
120 000 $ – 165 000 $ / metai
Darbas vietojeVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųVadovas

Lead medical device sales across a North Central New Jersey region, managing field teams and hospital relationships. Drive regional revenue, sales performance, and compliant promotion of Terumo Interventional Systems products.

Atidaryti