CRA II/Snr, Late Phase

Are you ready to be a part of a successful study delivery team? ICON's award-winning study execution capabilities have led to the approval of 18 of the world's top 20 best-selling drugs. Make your experience count for the benefit of patients worldwide. www.iconplc.com

ICON is hiring talented professionals in China as our China teams are growing!

CRA II, Snr - Late Phase, Real World Evidence

Location : Taipei, Taiwan

ICO invites you to learn more about our Late Phase CRA opportunity in Phases III-IV. We are seeking a Late Phase CRA with a desire to work on study teams that are often virtual,multi-cultural, and multi-disciplinary. Visit our web page to learn more about ICON Commercialisation &Outcome Services; https://www.iconplc.com/services/commercialisation-and-outcomes

The Late Phase CRA is responsible for managing,implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations. This specific role will have a significant focus on Medical Device studies. The responsibilities of this position include, but are not limited to:

-Identifying,training/initiating and closing out study sites.

-Conducting remote site monitoring visits and/or targeted on-site visits as needed.

-Conducting remote site management activities.

-Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.

The ideal candidate for this role will have a blend of the below knowledge and expertise:

- Bachelor's degree in a related field such as Life Sciences, Medicine, Clinical Trial, etc. or equivalent.

- 2+ year of blended inhouse and onsite monitoring experience.

-About 30% travel requirement for onsite visits on average.

-Prior exposure to Study Start Up activity would be beneficial including exposure to Ethic Committee and -Regulatory Authority Submissions within Taiwan

-Good command of English languages written and spoken.

-Late Phase Clinical Trial experience a prerequisite.