SSUA II or Sr SSUA - home based or office based

"At ICON, it's our People that set us Apart"

Are you interested in improving your knowledge of Clinical Trials and contributing to our culture of process improvement with a focus on streamlining our processes of adding value to our business and meeting client needs?

The CIC team serve as the primary liaison for the development of patient Informed Consent for assigned clinical studies. Responsibilities will include but are not limited to:

Development and Authoring of study level informed consent masters in accordance with client specific requirement o Liaising with ICON and sponsor study teams where required.

Review and approval of country and site level informed consent in accordance with client specific requirements o ensuring any legal or sponsor mandatory text requirements are adhered to o Liaising with ICON and sponsor teams where required.

Provide guidance and leadership to the study team in relation to Informed Consent process and development. Ensuring timely review and tracking of consents to meet established study timeline and required metrics. Involvement in the development of sponsor and ICON specific guidance and training.

Selected to coordinate clinical trial start-up activities and serve as primary contact for investigators and research coordinators in corporate sponsored human clinical trials.

The successful candidate will show capability in the areas of Clinical Trial operations, meeting regulatory and ICON guidelines and displaying project management skills. You will have experience of independently submitting applications to the ethics committees and Regulatory authorities, ideally with site contract negotiation experience.

We provide a Study Start Up Associate with the resources to be successful and visibility by having them provide input and recommendation to upper management on the study start up submission process and how to better the work process. In addition, we offer competitive pay, generous time off and bonus incentives

A high school diploma or local equivalent, Bachelor’s Degree preferably in life sciences will ensure your familiarity with regulatory guidelines and industry knowledge. Experience of independent clinical start up activities.

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.