
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.
🔥 14 hours ago
🚗 Michigan – Remote
💵 $78.5k - $141k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor
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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.
• Considered as the primary point of contact for the investigative site • Conducts site evaluation, site training, routine, and site closure monitoring activities • Aligns, trains and motivates the site staff and principal investigator • Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey • Ensures quality of data submitted from study sites • Protect study subjects' safety • Manages investigator payments as per executed contract obligations
• Minimum of 1 year of clinically related experience • 6 months required in clinical research monitoring of investigational drug or device trials • Familiar with risk‐based monitoring approach • Knowledge of appropriate therapeutic area indications is preferred • Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies • Strong cross-functional collaboration skills among internal and external stakeholders • Advanced ability to leverage technology, tools and resources
• medical/dental/vision insurance • 401(k) to eligible employees • paid time off (vacation, holidays, sick) • participate in short-term incentive programs
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