Learn More at: IQVIA.com
Connect with Us:

Clinical Trial Assistant (Taipei- March/April) - (1802661) in Taipei, TW at IQVIA™

Date Posted: 1/25/2018

Job Snapshot

Job Description

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
IQVIA™ pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster. If that is your passion, we have a place for you.

 
We are looking for suitable individuals to fill the position of :
 
Clinical Trial Assistant
 
Job Responsibilities:
• Assist the clinical team with updating and maintaining clinical systems that track site compliance and performance within project timelines
• Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures   
• Assist with periodic review of study files for accuracy and completeness
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• May perform assigned administrative tasks to support team members with clinical trial execution.

Job Requirements

Requirements:
• Minimum Diploma or equivalent with at least 2-3 years experience in administration
• Proficient in Microsoft Office (Excel, Word, Powerpoint, Outlook)
• Meticulous and able to work in a fast-paced environment
• English fluent in verbal and writtenWe know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™. Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.



Job ID: 1802661