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Clinical Research Associate II

🔥 16 hours ago

🌽 Illinois – Remote

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đź’µ $84.5k - $162k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

đź§Ş Clinical Research

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

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đź‘» Ghost score 0%

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AbbVie

10,000+ employees

Founded 2013

🏥 Healthcare

đź’Ľ 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.

đź“‹ Description

• 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 clinical trial goals, protocols, and patient treatment principles • Conduct site evaluation, training, routine monitoring, and site closure activities in compliance with protocols, regulations, GCPs, ICH Guidelines, SOPs, and quality standards • Customize site engagement strategies and gather local/site insights • Use CRM tools to report and track progress and measure strategy impact • Connect study protocols, scientific principles, and clinical trial requirements to daily trial execution • Evaluate recruitment and retention techniques based on the patient disease journey • Develop therapeutic area, asset, clinical landscape, and patient journey knowledge • Mentor and train less experienced CRAs • Participate in global/local task forces and initiatives • Conduct continuous risk assessment with the Central Monitoring team • Resolve site risk signals and implement preventative and corrective action plans • Identify and evaluate potential investigators and sites • Ensure quality and timely submission of site data and safety-event reporting • Maintain audit and regulatory inspection readiness • Manage investigator payments according to executed contracts

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred • Minimum of 1 year of clinically related experience • At least 6 months of clinical research monitoring experience for investigational drug or device trials • Familiarity with risk-based monitoring, onsite and offsite monitoring • Knowledge of therapeutic area indications preferred • Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Strong cross-functional collaboration, planning, organizational, interpersonal, written, verbal, active listening, and presentation skills • Ability to leverage technology, tools, and resources • Ability to apply critical thinking and good judgment to address clinical site issues • Integrity in accordance with AbbVie code of business conduct and leadership values • Self-motivated and able to deliver timely, quality outcomes in a fast-paced environment

🏖️ Benefits

• Paid time off including vacation, holidays, and sick leave • Medical, dental, and vision insurance • 401(k) • Short-term incentive programs • Remote work option • Equal opportunity employer benefits for veterans and disabled applicants

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