Senior CRA- ICO

At ICON we challenge and value our employees as they work towards excellence. We are looking for passionate , resilient and inspiring individuals to join our team.

As a top 5 CRO in the world, we are looking to strengthen our Clinical Operations team in the US. We empower our CRA's to work independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.

We empower our CRA's to work independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.

There is no limit to what you can achieve at ICON.  From contributing to the development of life-saving drugs to working in a team of dedicated experts, your work is always valued.  Teamwork is actively encouraged within our CRA group.  We value commitment to excellence and promote this across every element of the business.  Our CRAs are engaged and motivated to do their best every day.

Working for ICON you will be provided with a comprehensive benefits package including competitive salary, bonus, 401K with employer match, generous PTO, paid holidays, company cell phone, FSA and college savings plan..

We provide equal opportunity to all qualified applicants and employees by prohibiting discrimination in employment decisions because of race, color, religion, sex, national origin, age, veteran status or disability.