Are you an exceptional Clinical Research Associate (CRA) based in Hong Kong that has independent trial site monitoring experience and would like to experience working as a CRA at a global CRO?
Clinical Research Associates manage all aspects of study site monitoring according to Client SOP, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.
-Responsible for all aspects of study site visits and site management and monitoring activities ex. f/u SAE, clinical supply, etc
-Prepare accurate and timely trip report
-review progress of projects and initiate appropriate actions to achieve targets
-feasibility work, site selection, EC submission, RA submission, translation of study documents, negotiate study budget, contract
-University degree with pharmacy or medical related background preferred
-candidate with 2 or more relevant CRA experience in pharma or CRO
-thorough knowledge of ICH GCP and regulatory
-Fluent in local language and English
- 2 or more years CR experience in pharma or CRO
- Excellent monitoring skill, site management skill, communication skills
- Ability to work independently
- Good planning and organization skill, computer skills