CRA II

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 support our CRAs with manageable sites & protocols, a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and eligible for the annual performance bonus. Additionally, we have cutting edge technology to ensure better outcomes.

Successful candidates will possess:

· Bachelor's degree in a life science or related discipline OR RN/LPN with 4 years related experience.

· 12-24 months of onsite monitoring experience

· Strong understanding of ICH GCP Compliance

· Ability to travel 65-75% of the month

Benefits of working with ICON 

In addition to partnering with the top pharmaceutical and biotech companies in the world we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, bonus plans, vacation, and other incentives. 

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.