CRA

招聘人数：若干 到岗时间：不限 年龄要求：不限 婚况要求：婚姻状况 Assist Clinical Research Manager with the identification and selection of investigators to undertake clinical studies, when required.
Assist Clinical Research Manager with preparation of study budget.
Prepare documentation for Ethics Committee submission.
Coordinate receipt and distribution of clinical trial supplies.
Prepare and conduct initiation visits.
Oversee assigned clinical trials to ensure compliance.
Monitor and document the progress of assigned clinical studies through regular visits and telephone contact with site personnel.
Liaise with and report to Clinical Research Manager regularly on study status through monitoring reports and meetings.
Document all study related communications, newsletter etc.
Perform Source Data Verification to ensure accurate data is recorded.
Ensure all Serious Adverse Cardiac Events are reported and followed up.


Bachelor degree or above in Medicine or related field.
At least 1 year experience as a CRA.
Good working knowledge of GCP guidelines.
Proficiency in Microsoft Word and Excel and familiarity with use of database.
Knowledge of clinical trial methodology.
Result oriented.
Customer focus and teamwork.
Good communication skill, self-learning skill.
Proficient English & Chinese in both verbal and written.
Regional travel is required.