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AbbVie
AbbVie
H1B vīzas sponsorsKonsultācijasRažošanaVeselības aprūpe
AbbVie ir globāls farmācijas uzņēmums, kas koncentrējas uz zāļu atklāšanu, izstrādi un piegādi sarežģītu veselības traucējumu ārstēšanai. Tā produktu portfelis aptver imunoloģiju, onkoloģiju, neirozinātni un estētiku, un uzņēmums darbojas vairāk nekā 175 valstīs, nodrošinot pakalpojumus pacientiem visā pasaulē. Uzņēmuma darbība apvieno farmācijas pētniecību, ražošanu un veselības aprūpes kompetenci, ko papildina ievērojamas investīcijas zinātniskajās inovācijās, pētniecībā un izstrādē. AbbVie savā plašākajā pieejā veselības rezultātu un ietekmes uz kopienām uzlabošanai izceļ arī daudzveidību, ilgtspēju un pacientu atbalstu.
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Vakances uzņēmumā

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.

USAmerikas Savienotās ValstisCAKalifornija
75 000 $ – 142 500 $ / gads
AttālinātiPilna slodzeJaunākais speciālistsVidējais līmenisGrāds nav nepieciešamsNepieciešamā Valoda: angļuKlīniskā pētniecība
Google Cloud Platform

Apraksts

  • 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.

Prasības

  • 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.

Priekšrocības

  • 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.

Saistītās vakances

Emory University

Clinical Research Coordinator II – PFAS Study

Emory University
H1B vīzas sponsorsIzglītībaVeselības aprūpeZinātne
USAmerikas Savienotās ValstisHibrīdiPilna slodzeJaunākais speciālistsGrāds nav nepieciešamsNepieciešamā Valoda: angļuKlīniskā pētniecība

Coordinate field operations for Emory University’s North Georgia PFAS exposure-reduction study. Responsibilities include participant visits and consent, questionnaires, biological specimens, and study records.

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Syneos Health

Senior Clinical Research Associate (CRA II) – Seoul

Syneos Health
H1B vīzas sponsorsKonsultācijasLoģistikaVeselības aprūpe
KRDienvidkorejaHibrīdiPilna slodzeVecākais speciālistsNepieciešamā Valoda: angļuKlīniskās operācijas
Google Cloud Platform

Monitor clinical trial sites for Syneos Health across South Korea, supporting GCP compliance, data quality, recruitment, and audit readiness. This hybrid clinical operations role combines site oversight with collaboration across study teams.

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ICON plc

Senior Clinical Research Associate, Oncology (France, Remote)

ICON plc
KonsultācijasLoģistikaVeselības aprūpe
FRFrancijaAttālinātiPilna slodzeVecākais speciālistsNepieciešamā Valoda: angļuKlīniskā pētniecība
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Monitor oncology trials for ICON Strategic Solutions, overseeing site performance, protocol compliance, data quality, and regulatory standards. Support reliable trial conduct through site visits, team collaboration, and guidance for site staff and CRAs.

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Emory University

Clinical Research Coordinator I – Environmental Health Study

Emory University
H1B vīzas sponsorsIzglītībaVeselības aprūpeZinātne
USAmerikas Savienotās ValstisHibrīdiPilna slodzeJaunākais speciālistsGrāds nav nepieciešamsNepieciešamā Valoda: angļuKlīniskā pētniecība

Coordinate participant visits, consent, questionnaires, specimens, and field operations for Emory University’s study of chemical exposures and health outcomes. Serve as the study’s primary field contact in Glynn County, Georgia.

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Partnerize

Remote Site Reliability Engineer at Partnerize

Partnerize
201 – 500 Darbinieki
B2BMārketingsSaaS
USAmerikas Savienotās ValstisPAPensilvānijaAttālinātiPilna slodzeVidējais līmenisVecākais speciālistsNepieciešamā Valoda: angļuDevOps inženieris
AnsibleApacheAWSDockerElasticsearchKafkaKubernetesLinuxMākonisMySQLNGINXPHPPostgresPythonRedisTerraform

Help keep Partnerize’s partnership automation platform dependable by strengthening its cloud infrastructure, software delivery, and operational support.

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Summit Therapeutics, Inc.

Director of Clinical Operations Analytics and Performance Excellence

Summit Therapeutics, Inc.
201 – 500 Darbinieki
KonsultācijasMārketingsVeselības aprūpe
USAmerikas Savienotās Valstis
190 000 $ – 237 000 $ / gads
AttālinātiPilna slodzeVadošais speciālistsNepieciešamā Valoda: angļuKlīniskās operācijas
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Lead analytics and performance improvement for global oncology trials at Summit Therapeutics. Oversee Veeva Vault Clinical, data governance, portfolio reporting, and operational excellence.

Atvērt