Clinical Data Coordinator III

Are you passionate about improving the quality of human life? If so, we invite you to learn more about our Clinical Data Coordinator opportunities in the U.S..

ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutical organizations on emerging therapeutic areas which include but are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain.

We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally. We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients.
Overview of the Role

Independently and accurately review Case Report Form data for completeness, accuracy and consistency in accordance with all applicable procedures.
Accurately and consistently apply data handling conventions to Case Report Forms as necessary in accordance with all applicable procedures.
Perform Quality Reviews and appropriately address all issues.
Compile and distribute necessary study documentation and maintain accurate and complete study files in accordance with all applicable procedures.
Identify and appropriately address data discrepancies in the clinical data via computerized edits and manual checks/listings.
Assist with the development, review and the update of relevant Data Management Study Specific Procedures.

Education and /or Experience:

Minimum of a Diploma or Degree in a Scientific discipline or equivalent work experience.
Minimum of 1 year Clinical Data Management experience.


We invite you to review our opportunities at www.iconplc.com/careers.

 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.

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