Clinical Research Associate II

🔥 17 minutes ago

🇨🇳 China – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 Ghost score 10%

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AbbVie

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Advance AbbVie’s clinical pipeline through excellence in clinical research • Partner with investigators and site staff to support meaningful clinical-trial engagements • 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 in compliance with protocols, monitoring plans, regulations, GCP, ICH Guidelines, SOPs, and quality standards • Develop and customize site-engagement strategies for assigned studies • Gather local and site insights and use CRM tools to track progress and measure impact • Evaluate recruitment and retention techniques based on the patient disease journey • Build 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/local task forces and initiatives as assigned • Conduct continuous risk assessment with the Central Monitoring team to identify study-performance or patient-safety issues • Resolve site risk signals and implement preventative and corrective action plans • Identify, evaluate, and recommend potential investigators and sites • Ensure data quality and timely submission, including 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

🎯 Requirements

• Minimum of 1 year of clinically related experience • At least 6 months of clinical research monitoring of investigational drug or device trials • Familiarity with risk-based monitoring approach, onsite and offsite monitoring • Knowledge of appropriate therapeutic area indications preferred • Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies • Strong cross-functional collaboration skills among internal and external stakeholders • Strong planning and organizational skills; ability to work effectively in a dynamic environment with competing projects and deadlines • Advanced ability to leverage technology, tools, and resources for customer-centric site support • Strong interpersonal skills with excellent written, verbal, active listening, and presentation skills • Ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training • Ability to use functional expertise, critical thinking, and good judgment to address clinical site issues • Acts with integrity in accordance with AbbVie code of business conduct and leadership values • Self-motivated and focused on delivering timely, quality outcomes • Appropriate tertiary qualification in a health-related discipline (Medical, Scientific, Nursing) preferred

🏖️ Benefits

• Employees can work remotely • Equal opportunity employer • Reasonable accommodation for US & Puerto Rico applicants