CRA II
TA Business Partner
About the role
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This is an exciting opportunity to join ICON
re 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 - Late Phase, Real World Evidence
Location : China
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+ years 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 China.
-Fluent English languages written and spoken.
-Late Phase Clinical Trial experience a prerequisite.
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
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