Clinical Research Associate
2 dagen geleden
The Clinical Trials Centre (HKU-CTC) is a leading clinical trials management platform established under the LKS Faculty of Medicine. We are seeking a highly skilled Clinical Research Associate to join our Project Operations Unit (POU) in Hong Kong.
Main Responsibilities:- Act as a key contact person among clinical study centres, sponsoring companies, regulatory authorities, and other stakeholders.
- Facilitate the planning, initiation, and monitoring of clinical studies throughout their project life cycles.
- Assess the feasibility of clinical studies.
- Support study planning, preparation, and initiation.
- Monitor the progress and quality of study activities.
- Oversee study centres' compliance with study protocols, Good Clinical Practice (GCP), and other research ethics and regulatory requirements.
- Assist in the proper closure of clinical studies.
- Facilitate study audits and inspections as needed.
- Bachelor's degree or above in Health, Biological/Life Sciences, Medical, Pharmacy, Nursing, or related disciplines.
- Experience in clinical research operations and development.
- Good interpersonal and communication skills.
- Good coordination and problem-solving skills.
- Detail-minded and able to handle multiple concurrent tasks.
- Good command of written and spoken English and Cantonese.
A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits. The appointment will commence as soon as possible for one or two years, renewable subject to satisfactory performance.
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Utrecht, Utrecht, Nederland PRA Voltijd{"title": "Clinical Research Associate", "content": "Role SummaryAt PRA, we're committed to advancing and improving patients' lives through our work in clinical research. As a Clinical Research Associate, you'll play a critical role in ensuring the success of our studies by providing site management and monitoring services.Key ResponsibilitiesProvide site...
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