Job Description
Our client is a global clinical research organization, currently seeking an (Senior) Clinical Research Associate to join their innovative for site management and monitoring responsibilities in clinical studies. The role offers excellent career exposures, focusing on accelerating drug development and novel clinical trials. If you are seeking opportunities to contribute to advance scientific research through clinical studies and pharmaceutical development, this is an excellent position for you.
Key Responsibilities
- Manage clinical on-site activities for clinical trials, including pre-study, monitoring, and close-out visit according to company’s standard the clinical guidelines.
- Verify informed consent procedures and compliance with protocol requirements.
- Conduct source document review and data verification to ensure accuracy and completeness.
- Maintain regulatory documents and investigational product accountability.
- Prepare project plans and ensure adherence to quality control metrics.
- Perform eCRF reviews, track adverse events, and assist in investigator and patients recruitment.
Key Requirements:
- Bachelor’s degree or above in Biomedical Science, or related life science academic qualifications
- Strong understanding of ICH-GCP Guidelines, local regulatory requirements, Serious Adverse Event reporting
- Thorough knowledge of clinical monitoring procedures and clinical trail process.
- Fluent in English, Cantonese and Mandarin
- Minimum of a year of clinical monitoring experience is preferred.
- Familiarity of e-clinical systems
- Strong team worker and good communication skills
What to do now?
If you are eager to contribute to meaningful advancements in clinical sectors and thrive in a collaborative environment, we invite you to apply and become a vital part of our client's mission to improve patient outcomes. Alternatively, send your latest CV to tiffany.wong@linksinternational.com for confidential chat of your career and know more about the Hong Kong pharmaceutical market!