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AbbVie
AbbVie
Sponsor pentru viza H1BAsistență medicalăConsultanțăIndustria prelucrătoare
AbbVie este o companie farmaceutică globală axată pe descoperirea, dezvoltarea și furnizarea de medicamente pentru afecțiuni complexe. Portofoliul său acoperă imunologia, oncologia, neuroștiința și medicina estetică, iar operațiunile sale deservesc pacienți din peste 175 de țări. Activitatea companiei combină cercetarea farmaceutică, producția și expertiza în domeniul sănătății, susținute de investiții substanțiale în inovarea științifică și cercetare și dezvoltare. AbbVie pune, de asemenea, accent pe diversitate, sustenabilitate și sprijinirea pacienților, ca parte a abordării sale mai ample pentru îmbunătățirea rezultatelor în domeniul sănătății și a impactului asupra comunităților.
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Locurile de muncă ale companiei

Clinical Research Associate I – Neurology, Florida Remote

Support AbbVie’s neurology clinical trials through investigative-site monitoring, compliance oversight, data-quality management, and patient-safety activities. Help maintain study performance from site evaluation and training through monitoring, risk management, and closeout.

USStatele Unite ale AmericiiFLFlorida
75.000 $ – 142.500 $ / an
RemoteNormă întreagăJuniorNivel mediuNu este necesară o diplomăLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • Support the execution of AbbVie’s neurology clinical research pipeline
  • Act as the primary contact for investigative sites
  • Connect stakeholders with investigative sites while providing clinical-trial context
  • Train, align, and motivate site staff and principal investigators on trial goals, protocols, and patient-treatment principles
  • Perform site evaluation, training, routine monitoring, and closeout activities under supervision
  • Maintain adherence to protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards
  • Tailor site-engagement strategies and measure their effectiveness with CRM tools
  • Apply protocol, scientific, and clinical-trial expertise to daily study execution
  • Assess recruitment and retention approaches in relation to the patient disease journey
  • Build knowledge of the therapeutic area, development assets, clinical landscape, and patient journey
  • Perform ongoing risk assessments with the Central Monitoring team
  • Address site risk signals and put preventive and corrective action plans into effect
  • Identify, assess, and recommend investigators and sites under supervision
  • Ensure site data and safety-event reports are accurate and submitted on time
  • Keep studies prepared for audits and regulatory inspections
  • Administer investigator payments in line with executed contract obligations

Cerințe

  • A relevant tertiary qualification in medicine, science, nursing, or another health discipline is preferred; equivalent experience may be considered
  • Clinically relevant experience, ideally in clinical research coordination or data management
  • Familiarity with relevant therapeutic-area indications is preferred
  • Understanding of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies
  • Ability to collaborate effectively across teams and functions
  • Strong planning and organizational skills, including the ability to manage competing projects and deadlines
  • Ability to use technology, tools, and available resources effectively
  • Critical-thinking and sound judgment when addressing clinical-site issues
  • Strong written, verbal, active-listening, and presentation skills
  • Ability to build site relationships and trusted partnerships
  • Commitment to integrity under AbbVie’s code of business conduct and leadership values
  • Self-directed approach with a focus on timely, high-quality outcomes
  • Ability to work remotely

Beneficii

  • Paid time off, including vacation, holidays, and sick leave
  • Medical, dental, and vision insurance
  • 401(k) plan
  • Short-term incentive programs
  • Equal-opportunity benefits for veterans and people with disabilities
  • Reasonable-accommodation support for applicants in the United States and Puerto Rico

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