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AbbVie is a global pharmaceutical company focused on discovering, developing, and delivering medicines for complex health conditions. Its portfolio spans immunology, oncology, neuroscience, and aesthetics, with operations serving patients in more than 175 countries. The company’s work combines pharmaceutical research, manufacturing, and healthcare expertise, supported by substantial investment in scientific innovation and research and development. AbbVie also highlights diversity, sustainability, and patient support as part of its broader approach to improving health outcomes and community impact.
Clinical Research Associate II Remote China
Support AbbVie’s oncology clinical trials remotely from China through site monitoring, patient-safety oversight, and high-quality clinical data management.
Description
- Support AbbVie’s clinical development pipeline through high-quality clinical research delivery
- Collaborate with investigators and site teams to promote effective trial engagement
- Act as the main contact for investigative sites
- Provide relevant trial information and connect stakeholders with investigative sites
- Align, train, and motivate site teams and principal investigators on trial objectives, protocols, and patient-treatment principles
- Perform site selection, training, routine monitoring, and closeout in accordance with protocols, monitoring plans, regulations, GCP, ICH guidelines, AbbVie SOPs, and quality standards
- Tailor site-engagement strategies and use CRM tools to track progress and assess impact
- Apply protocol, scientific, and clinical-trial expertise to daily study execution
- Assess recruitment and retention strategies in relation to the patient disease journey
- Build therapeutic-area, asset, clinical-landscape, and patient-journey knowledge to support recruitment and protocol adherence
- Mentor and train junior CRAs and support their professional development
- Contribute to global and local task forces and initiatives
- Partner with Central Monitoring to continuously assess risks affecting study performance or patient safety
- Address site risk signals and implement preventive and corrective action plans
- Identify and assess prospective investigators and clinical sites
- Protect data quality, ensure timely data submission, and support appropriate safety-event reporting and follow-up
- Keep assigned sites prepared for audits and regulatory inspections
- Administer investigator payments in line with executed contract obligations when applicable
Requirements
- A tertiary qualification in a health-related field such as medicine, science, or nursing is preferred
- At least one year of clinically related experience
- At least six months of clinical research monitoring experience on investigational drug or device trials
- Familiarity with risk-based monitoring, including on-site and remote 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 collaboration skills for working with internal and external stakeholders
- Strong planning and organizational ability, with the capacity to work efficiently in a dynamic environment with competing deadlines
- Advanced ability to use technology, tools, and resources to provide site-focused support
- Strong interpersonal, written, verbal, active-listening, and presentation skills
- Ability to build and maintain trusted site partnerships through engagement, motivation, and training
- Ability to use critical thinking and sound judgment when addressing clinical-site issues
- Commitment to integrity in line with AbbVie’s code of business conduct and leadership values
- Self-motivated approach with a focus on timely, high-quality results in a fast-paced environment
Benefits
- Remote work is available to employees
- AbbVie is an equal opportunity employer
- The company is committed to integrity, innovation, transforming lives, and serving the community
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