
10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
🔥 0 minutes ago
🇬🇧 United Kingdom – Remote
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🚫👨🎓 No degree required
🇬🇧 UK Skilled Worker Visa Sponsor
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10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
• Advance AbbVie’s clinical development pipeline by striving for excellence in clinical research and leveraging advanced capabilities • Serve as the primary point of contact for investigative sites • Provide contextual information on clinical trials and connect stakeholders with investigative sites • Align, train and motivate site staff and principal investigators on trial goals, protocols and patient treatment principles • Conduct site evaluation, site training, routine monitoring and site closure activities • Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs and quality standards • Customize site engagement strategies and use CRM tools to track progress and measure impact • Connect study protocols and scientific principles to day-to-day trial execution • Evaluate recruitment and retention techniques based on the patient disease journey • Develop therapeutic-area, asset, clinical-landscape and patient-journey knowledge to support recruitment and protocol compliance • Mentor and train less experienced CRAs and contribute to their development • Participate in global or local task forces and initiatives • Conduct continuous risk assessment with the Central Monitoring team to detect study-performance or patient-safety issues • Resolve site risk signals and implement preventative and corrective action plans • Identify, evaluate and recommend potential investigators and clinical trial sites • Ensure quality and timely submission of site data, safety-event reporting and follow-up • Maintain audit and regulatory inspection readiness at assigned sites • Manage investigator payments according to executed contract obligations, as applicable
• Appropriate tertiary qualification in health-related disciplines such as Medical, Scientific or Nursing is preferred • Minimum of 1 year of clinically related experience • At least 6 months of clinical research monitoring experience involving investigational drug or device trials • Familiarity with risk-based monitoring, including onsite and offsite monitoring • Knowledge of relevant therapeutic-area indications is preferred • Ability to understand and apply scientific concepts to clinical trial conduct • Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies • Strong cross-functional collaboration skills • Strong planning and organizational skills; ability to manage competing projects and deadlines • Advanced ability to leverage technology, tools and resources • Strong interpersonal, written, verbal, active listening and presentation skills • Ability to establish site relationships and trusted partnerships through engagement, motivation and training • Ability to apply critical thinking and good judgment to clinical-site issues • Integrity aligned with AbbVie’s code of business conduct and leadership values • Self-motivated and focused on timely, quality outcomes in a fast-paced environment
• Employees can work remotely • Equal opportunity employer • AbbVie is committed to operating with integrity, driving innovation, transforming lives and serving the community
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