Study Start Up Associate II ( Clinical Site Activation Associate)

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Role:

Study Strat Up Associate II (Clinical Site Activation Associate)

Summary:

Participate on clinical trial Start Up activities by understanding the clinical site activation requirements and assist the sites in their progress, ensuring that site activation is executed according to plans.

Responsibilities:

• Oversees day to day execution and site progress for all aspects and tasks related to site activation for the assigned projects and sites.

• Assist and engage with sites to ensures that site staff team members are progressing throughout site activation in accordance with the site activation plans and in accordance with the site activation requirements, in an effective manner to meet sponsor timelines and expectations and in compliance with ICON/client KPIs, ICON/client SOPs.

• Support internal tools set up, maintenance and timely updates and ensure site adoption of ICON tools. Contribute to effective site activation process and timelines.

• Participate to internal study reviews with study teams to contribute to risk identification and contribute to action planning.

To be successful in the role, you will have:

• Bachelor’s Degree preferably in life sciences

• Minimum of 1 – 2 + years’ experience in Clinical Research environment (Experience as Senior CTA, IHCRA, CRA I is a plus)

• Project management skill set

• Understanding of regulatory and submission processes in many different countries

• Excellent English written and verbal communication

• Ability to work to tight deadlines