
10,000+ employees
Founded 2013
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
Pharmaceuticals • Biotechnology • Healthcare Insurance
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.
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10,000+ employees
Founded 2013
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
Pharmaceuticals • Biotechnology • Healthcare Insurance
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.
• Work independently as a clinical study leader and contributor • Support the Study Project Manager in strategic leadership of the cross-functional team • Manage vendor relationships and oversight of external vendors • Oversee recruitment management and execution of recruitment strategies • Ensure inspection readiness and participate in related activities • Manage study materials and ensure compliance/inspection readiness
• Bachelor’s Degree • At least 4 years of progressive Pharma-related/clinical research-related experience • Competent in application of standard quality procedures (SOP, ICH/GCP, Global Regulations) • Experienced user of systems such as EDC, IRT, CTMS, and eTMF • Strong analytical and critical thinking skills • Excellent organizational and time management skills • Exceptional interpersonal skills with ability to communicate effectively in English
• Health insurance • Flexible work arrangements
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