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McKesson
McKesson
H1B vizos rėmėjasKonsultavimasLogistikaSveikatos priežiūra

McKesson yra sveikatos priežiūros įmonė, veikianti farmacijos produktų platinimo, medicinos priemonių ir sveikatos priežiūros paslaugų srityse. Jos veikla padeda vaistinėms, klinikoms, sveikatos priežiūros sistemoms ir pacientams gauti būtiną gydymą, taip pat prisideda prie efektyvesnio sveikatos priežiūros veikimo ir atsparaus atsako į vaistų trūkumą.

Įmonė taip pat kuria vaistinių valdymo programinę įrangą ir teikia konsultavimo bei technologinius sprendimus specializuotoms praktikoms. McKesson bendradarbiauja su biofarmacijos organizacijomis ir remia onkologijos bei biofarmacijos praktikas, teikdama paslaugas, orientuotas į vaistų prieinamumą, pacientų gydymo laikymąsi, komercializaciją, duomenimis pagrįstas įžvalgas ir realaus pasaulio įrodymus.

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Darbai įmonėje

Research Regulatory Affairs Specialist – Tennessee

Support FDA, GCP, and IRB compliance for oncology clinical trials at Sarah Cannon Research Institute. Coordinate regulatory documentation and audit readiness with sponsors, research sites, and investigators in this remote Tennessee role.

USJungtinės ValstijosTNTenesisNuotolinisVisas etatasJaunesnysis specialistasDiplomas nebūtinasPrivaloma Kalba: anglųAtitiktis
Google Cloud Platform

Aprašymas

  • Plan regulatory compliance for industry sponsors and network research sites.
  • Partner with regulatory leaders and investigators to maintain compliance.
  • Prepare for audits while meeting demanding deadlines.
  • Set up and maintain electronic regulatory document systems.
  • Maintain FDA- and GCP-required records for sites, studies, sponsors, and networks.
  • Check regulatory documents against local procedures for format and content.
  • Keep essential compliance records current.
  • Revise or develop informed consent forms.
  • Manage protocol, investigator brochure, and consent form changes in line with IRB policy and HIPAA.
  • Coordinate time-sensitive communications with sponsors and other stakeholders.
  • Prepare and submit documentation to IRBs across multiple trials.
  • Process protocol deviations that meet IRB reporting criteria.
  • Send urgent safety notices to the IRB.
  • Carry out additional duties as assigned.

Reikalavimai

  • High school diploma or equivalent is required.
  • An associate degree or higher is preferred.
  • Relevant experience may substitute for education.
  • At least one year of regulatory affairs experience in clinical research, pharmaceuticals, or a site management organization is strongly preferred.
  • Knowledge of medical terminology is strongly preferred.
  • Knowledge of FDA and other regulatory processes is strongly preferred.
  • Ability to manage a full study workload with limited supervision.
  • Knowledge of IRB policies and HIPAA compliance.
  • Familiarity with FDA and GCP documentation requirements.
  • Ability to meet strict deadlines and prepare for audits.

Privalumai

  • A Total Rewards package with benefits supporting physical, mental, and financial well-being.
  • Competitive compensation.
  • Annual bonuses or long-term incentives may be available.
  • Equity may be part of compensation.
  • McKesson employee benefits.

Susiję darbai

Bloomlife Inc

Remote Account Sales Executive, Healthcare

Bloomlife Inc
11 – 50 Darbuotojai
Dirbtinis intelektasSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosNuotolinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųPardavimai

Grow Bloomlife’s remote maternal-fetal monitoring business by selling remote patient monitoring solutions to OB/GYN practices and health systems. Manage the full sales cycle, from prospecting and clinical presentations to contract negotiations and deployment handoffs.

Atidaryti
Illumina

Clinical Sales Specialist, Genomics — Thailand, Indonesia and Vietnam

Illumina
5 001 – 10 000 Darbuotojai
H1B vizos rėmėjasGamybaKonsultavimasSveikatos priežiūra
THTailandasNuotolinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųPardavimai

Support Illumina’s clinical genomics sales across Thailand, Indonesia and Vietnam, advising customers on applications, workflows and products. The role spans reproductive and genetic health, oncology, customer development and regional market growth.

Atidaryti
Trane Technologies

Senior Executive Assistant, Digital Leadership

Trane Technologies
B2BEnergetikaGamyba
USJungtinės ValstijosMNMinesotaNCŠiaurės Karolina
61 300 $ – 109 655 $ / metai
HibridinisVisas etatasVyresnysis specialistasVadovasPrivaloma Kalba: anglųVadovo asistentas

Support Trane Technologies’ Digital leadership team by coordinating executive schedules, travel, meetings, communications, and procurement. The role covers leaders across the United States and requires on-site work in White Bear Lake, Minnesota, Monday through Thursday.

Atidaryti