CRA I
RemoteChina
Job Summary
Partner with investigative sites as the primary point of contact to contextualize clinical trials and strengthen AbbVie's positioning. Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles. Conduct site evaluations, routine monitoring, and closure activities under supervision while ensuring compliance with Good Clinical Practices and applicable regulations. Customize engagement strategies for assigned studies, gather local insights, and track progress using CRM tools. Proactively assess risks, collaborate with the Central Monitoring team to detect early study performance or safety issues, and implement corrective action plans. Ensure data quality, timely submissions, and audit readiness at clinical sites. Manage investigator payments as per contract obligations.
Required Qualifications
- Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing)
- Clinically related experience, preferably in clinical research coordinating or data management
- Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies
- Ability to work collaboratively and cross functionally to develop and sustain working relationships
- Demonstrate planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines
- Interpersonal skills with strong written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training
- Acts with integrity in accordance with AbbVie code of business conduct and leadership values
- Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment
- US & Puerto Rico only
Desired Qualifications
- Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred
- Experience or equivalent work experience
- Knowledge of appropriate therapeutic area indications is preferred
- Ability to understand and apply scientific concepts as they relate to the conduct of clinical trials
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