LogoFresh Jobs Ahead
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.
LinkedIn
Darbai įmonėje

Principal Clinical Research Associate, FSP — South Korea Remote

Monitor Roche-sponsored clinical trials for a contract research organization, supporting site compliance, accurate data, complete documentation, and trial progress.

KRPietų KorėjaNuotolinisVisas etatasVyresnysis specialistasVadovasPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Aprašymas

  • Monitor investigator sites using a risk-based approach.
  • Analyze root causes and identify site process failures and corrective or preventive actions.
  • Review source data, source documents, and case report forms during on-site and remote monitoring to ensure data accuracy.
  • Check investigational products through physical inventory and records review.
  • Prepare timely observation reports and letters that meet business writing standards.
  • Escalate deficiencies and issues to clinical management and track them through resolution.
  • Stay in contact with investigative sites between visits to check protocol adherence, issue resolution, and timely data entry.
  • Support investigator payment processes and resolve findings with project team members.
  • Attend investigator meetings and work with the client to identify potential investigators.
  • Initiate trial sites in line with protocols, regulatory requirements, and ICH GCP obligations.
  • Close out trials and retrieve trial materials.
  • Check essential documents for completeness and conduct on-site file reviews.
  • Track trial status and report progress to the Clinical Trial Manager.
  • Maintain study systems, including the Clinical Trial Management System, in line with study conventions.

Reikalavimai

  • Hold a university degree in a science-related field.
  • Have at least seven years of independent monitoring experience in Phase I–III clinical development.
  • Understand ICH-GCP and KGCP requirements.
  • Be fluent in English.
  • Demonstrate clinical monitoring skills.
  • Understand medical or therapeutic areas and medical terminology.
  • Maintain working knowledge of ICH GCP, applicable regulations, and procedural documents.
  • Apply critical thinking, root cause analysis, and problem-solving skills.
  • Manage risk-based monitoring concepts and processes.
  • Communicate effectively in writing and verbally.
  • Demonstrate customer focus, listening skills, and attention to detail.
  • Organize work and manage time effectively.
  • Build effective working relationships.
  • Adapt flexibly to changing needs.
  • Work effectively both independently and as part of a team.
  • Use Microsoft Office confidently and learn relevant software.

Privalumai

  • Sign-on bonus.

Susiję darbai

Medtronic

Director of Clinical Research, Peripheral Nerve Stimulation

Medtronic
H1B vizos rėmėjasGamybaSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosMNMinesotaOHOhajas
212 800 $ – 319 200 $ / metai
Darbas vietojeVisas etatasVadovasPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Lead global clinical evidence programs for Medtronic’s Peripheral Nerve Stimulation therapies. Oversee studies, regulatory support, scientific publications, and collaboration across healthcare functions.

Atidaryti
MSD

Senior Principal Scientist, Gastrointestinal Oncology Clinical Research at MSD

MSD
H1B vizos rėmėjasBiotechnologijaLogistikaSveikatos priežiūra
USJungtinės ValstijosNJNaujasis DžersisPAPensilvanija
282 200 $ – 444 200 $ / metai
HibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųKlinikiniai tyrimai

Lead clinical development and trials for oncology medicines at MSD. Shape research strategy, analyze findings, support regulatory submissions, and work across scientific and business teams.

Atidaryti
Protiviti

Senior Forensic Investigations Consultant

Protiviti
5 001 – 10 000 Darbuotojai
H1B vizos rėmėjasFinansaiKibernetinis saugumasKonsultavimas
USJungtinės ValstijosMAMasačusetsasNYNiujorkas
94 000 $ – 140 000 $ / metai
HibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųAdvokatas
Kibernetinis saugumas

Lead fraud, forensic, and regulatory investigations at Protiviti, coordinating workstreams, evidence analysis, client deliverables, and junior staff development.

Atidaryti
Worldwide Clinical Trials

Senior Clinical Research Associate, Psychiatry

Worldwide Clinical Trials
1 001 – 5 000 Darbuotojai
H1B vizos rėmėjasKonsultavimasLogistikaSveikatos priežiūra
USJungtinės ValstijosFLFloridaPAPensilvanija
97 000 $ – 193 000 $ / metai
HibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųKlinikiniai tyrimai

Lead monitoring and site support for psychiatric clinical trials across the East Coast with Worldwide Clinical Trials. The role covers site selection, study start-up, compliance, data quality, and participant safety.

Atidaryti
Worldwide Clinical Trials

Senior Clinical Research Associate, Psychiatry and Alzheimer’s

Worldwide Clinical Trials
1 001 – 5 000 Darbuotojai
H1B vizos rėmėjasKonsultavimasLogistikaSveikatos priežiūra
USJungtinės ValstijosFLFloridaPAPensilvanija
97 000 $ – 193 000 $ / metai
HibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųKlinikiniai tyrimai

Monitor psychiatry and Alzheimer’s clinical trials for Worldwide Clinical Trials across East Coast sites. Oversee site visits, regulatory compliance, and data quality.

Atidaryti
GMS

Workers’ Compensation Subrogation and Civil Litigation Attorney

GMS
201 – 500 Darbuotojai
H1B vizos rėmėjasAparatinė įrangaGamybaKonsultavimas
USJungtinės ValstijosCAKalifornija
80 000 $ – 200 000 $ / metai
HibridinisVisas etatasJaunesnysis specialistasVidutinis lygisDiplomas nebūtinasPrivaloma Kalba: anglųAdvokatas

Associate attorney handling workers’ compensation subrogation claims and civil litigation for California employers, insurers, and self-insured businesses. The role is with GMS, a California defense firm.

Atidaryti