AbbVie murakkab sog‘liq muammolari uchun dori vositalarini kashf etish, ishlab chiqish va yetkazib berishga e’tibor qaratadigan global farmatsevtika kompaniyasidir. Uning portfeli immunologiya, onkologiya, nevrologiya va estetika yo‘nalishlarini qamrab oladi, faoliyati esa 175 dan ortiq mamlakatdagi bemorlarga xizmat ko‘rsatadi. Kompaniya faoliyati farmatsevtika tadqiqotlari, ishlab chiqarish va sog‘liqni saqlash sohasidagi tajribani birlashtiradi hamda ilmiy innovatsiyalar va tadqiqotlar hamda ishlanmalarga kiritiladigan katta investitsiyalar bilan qo‘llab-quvvatlanadi. AbbVie sog‘liq natijalari va jamiyatga ta’sirni yaxshilashga qaratilgan kengroq yondashuvining bir qismi sifatida xilma-xillik, barqarorlik va bemorlarni qo‘llab-quvvatlashni ham ta’kidlaydi.
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.
Tavsif
- 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
Talablar
- 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
Imtiyozlar
- 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