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AbbVie
AbbVie
H1B vizos rėmėjasGamybaKonsultavimasSveikatos priežiūra
„AbbVie“ yra pasaulinė farmacijos bendrovė, daugiausia dėmesio skirianti sudėtingoms sveikatos būklėms gydyti skirtų vaistų atradimui, kūrimui ir tiekimui. Jos produktų portfelis apima imunologiją, onkologiją, neuromokslus ir estetiką, o bendrovė veikia daugiau nei 175 šalyse, aptarnaudama pacientus visame pasaulyje. Įmonės veikla apima farmacinius tyrimus, gamybą ir sveikatos priežiūros kompetenciją, kurią stiprina didelės investicijos į mokslines inovacijas bei mokslinius tyrimus ir plėtrą. „AbbVie“ taip pat pabrėžia įvairovę, tvarumą ir pacientų rėmimą kaip platesnio požiūrio į sveikatos rezultatų ir poveikio bendruomenėms gerinimą dalį.
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Darbai įmonėje

Clinical Research Associate I, Neurology — California Remote

Support AbbVie’s neurology clinical trials by monitoring research sites and helping uphold regulatory compliance, data quality, patient safety, and recruitment goals.

USJungtinės ValstijosCAKalifornija
75 000 $ – 142 500 $ / metai
NuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisDiplomas nebūtinasPrivaloma Kalba: anglųKlinikiniai tyrimai
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Aprašymas

  • Support AbbVie’s clinical research pipeline and promote high standards in trial delivery.
  • Work with investigators and site teams to support effective clinical trial partnerships.
  • Act as the main contact for investigative sites.
  • Share clinical trial information and connect stakeholders with investigative sites.
  • Guide, train, and motivate site staff and principal investigators under supervision.
  • Carry out site assessments, training, routine monitoring, and closeout activities under supervision.
  • Help ensure adherence to protocols, monitoring plans, regulations, GCP, ICH guidelines, SOPs, and quality standards.
  • Tailor engagement plans for assigned study sites under supervision.
  • Collect local and site insights, and use CRM tools to track progress and assess impact.
  • Apply study protocols, scientific principles, and trial requirements to daily site work.
  • Assess and support patient recruitment and retention plans.
  • Build knowledge of the therapeutic area, study assets, clinical landscape, and patient journey.
  • Continuously assess risk with the Central Monitoring team.
  • Address site risk signals and clinical site issues.
  • Put preventive and corrective actions in place to reduce risk and support compliance.
  • Identify, assess, and recommend investigators and sites under supervision.
  • Support accurate, timely submission of site data and safety event reports.
  • Keep sites prepared for audits and regulatory inspections.
  • Administer investigator payments in line with executed contract terms.

Reikalavimai

  • A relevant tertiary qualification in a health discipline such as medicine, science, or nursing is preferred; equivalent work experience may also qualify.
  • Clinically related experience, preferably in clinical research coordination or data management.
  • Knowledge of indications in the relevant therapeutic area is preferred.
  • Knowledge of local regulatory and legal requirements, ICH/GCP guidelines, and applicable policies.
  • Ability to collaborate across teams and functions.
  • Strong planning and organizational skills.
  • Ability to work effectively in a changing environment with competing projects and deadlines.
  • Ability to make effective use of technology, tools, and resources.
  • Critical thinking and sound judgment.
  • Strong written, verbal, listening, and presentation skills.
  • Ability to build and maintain site relationships and trusted partnerships.
  • Integrity and conduct aligned with AbbVie’s business code and leadership values.
  • Self-motivation and focus on timely, high-quality results.
  • Work authorization in the United States is implied by the US-based role and applicant provisions.

Privalumai

  • Paid leave, including vacation, holidays, and sick time.
  • Medical, dental, and vision insurance.
  • 401(k) plan.
  • Short-term incentive programs.
  • Equal opportunity employer.
  • Reasonable accommodations for applicants.
  • Employment practices inclusive of veterans and people with disabilities.

Susiję darbai

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.

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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.

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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.

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