Description
We are seeking a Clinical Research Coordinator to join our team.
As a Clinical Research Coordinator, you will work as a research team member, following regulatory requirements, agreed-upon scope of work, applicable Standard Operating Procedures (SOPs), work authorization, and study protocols at the research site.
Key responsibilities include:
- Assisting researchers with feasibility questionnaires and retrieving completed questionnaires
- Facilitating study site initiation, including screening visits, submitting documents to ethics committees for approval, and dispensing investigational products
- Supporting researcher with subject screening and enrollment
- After obtaining researcher authorization, assisting with follow-up visits and procedures as required by the protocol, such as planning, verifying medication inventory, and coordinating activities
- Managing investigational products, study materials, and laboratory samples at the research site
- Participating in investigator meetings, monitoring visits, audits, and other meetings within the agreed scope of work
- Assisting researchers with archiving study documents and submitting them to ethics committees or other regulatory authorities
- Accurately transferring data from source documents to case report forms and assisting with query resolution
- Coordinating study site closure activities, including closing visits, retrieving investigational products and study materials, and archiving study documents
- Creating and maintaining routine work reports and other work-related documents
- Providing training and support to researchers and other clinical trial personnel, such as nurses and laboratory technicians
Requirements:
- Knowledge of clinical development and regulatory requirements
- Familiarity with medical terminology
- Strong interpersonal and organizational skills
- Proficiency in Microsoft Office software
- Fluent Chinese speaking and writing skills, with basic English proficiency
- Ability to work independently, prioritize tasks, and solve problems
- Strong confidentiality and integrity
- Bachelor's degree in Clinical Medicine, Pharmacology, Nursing, Healthcare, or related fields
- University English proficiency certificate (Band 4 or above)
IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud.