As a top five Clinical Research Organization in the world, we are looking to strengthen our Clinical Operations team in the US.. As a CRA you will work independently and actively handle 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.
You will be supported 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 innovative technology and provide excellent training to ensure better outcomes.
You will possess:
Bachelor’s degree in a life science or related discipline OR RN/LPN with related experience.Minimum of 1 year of active independent field monitoring experience in the USOncology monitoring experience is a plusLive anywhere in the US, not just in Raleigh, NC. This is a home-based position.Deep understanding of ICH GCP Compliance.Excellent time management and social skillsHighly motivated with a phenomenal eye for detail.Ability to travel 60 – 80% of the month.
Benefits of working with ICON:Comprehensive benefits package including premium salaryBonus401K with employer matchPaid holidaysCompany cell phone and equipment
We care about our people and your passion, as they are the key to our success and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term career. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of ICON.