Taiwan Clinical Research Associate

Proclinical is seeking a Clinical Research Associate for a global CRO to be based in Taiwan on a permanent basis.

Job Responsibilities:

• Conduct and report all types of onsite monitoring visits
• Be involved in study start-up
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

Skills and Requirements:

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• At least 2 years of Independent on-site monitoring experience in Taiwan
• Experience in all types of monitoring visits in Phase II and/or III
• Prior exposure to project start-up activities, including regulatory submissions
• Experience in Oncology, Haematology, Infectious Diseases, Gastroenterology and/or Neurology
• Experience of working with Hong Kong and/or Chinese Investigators and sites is a plus
• Full working proficiency in English
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Mandy Fang at m.fang@Proclinical.com or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

EA13C6865 | R1215238

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