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CRA II

Seoul
Permanent
Reference: 059705_1572488049
Description

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 Korea as our Korea teams are growing!

CRA II, Real World Evidence(Late Phase)

Location : Seoul,Korea

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 Korea.

-Fluent English languages written and spoken.

-Late Phase Clinical Trial experience a prerequisite.

Benefits of Working in ICON

In comparison with our competitor's and pharmaceutical companies, we provide more flexible and reasonable working platforms for coaching and educating new comer's to be highly respected professionals in our industry. ICON also provides successful candidates with an excellent employment package and benefits adapted to the current job market. We are more like an extended family with consideration of staff as individuals allowing a work-life balance.

Additionally, we have cutting edge technology that will allow you to analyze study specific processes, audit reports, and governance to quality system checks and ensure compliance.

What's Next
Following your application, if you have the necessary skills and experience for this job you will be invited to an initial telephone interview with one of our dedicated recruiters who will be able to provide you with more details of this opportunity.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment
We care about our people, since 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
We are an equal opportunity employer and value diversity at our company We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status

 

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