SMA II

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

As a Site Management Associate at ICON, you'll be responsible for managing, implementing and monitoring clinical studies in a team setting.

The Role

• Identifying, training/initiating and closing out study sites

• Conducts and completes remote site management activities, with support as needed, according to the Site Management Plan.

• Manage study sites and required protocols, amendments and deviations.

• Assure data is reported accurately and timeline are maintained.

• Serves as the primary contact for sites and investigates participating in studies.

• Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others) and other site management documents.

• Review drug storage and drug accountability procedures in accordance with applicable SOPs.

What you need

• Bachelor's degree or local equivalent in medicine, science or related discipline.

• Minimum of one year of relevant experience in a health care or research environment strongly preferred.

• Ability to review and evaluate clinical data

• Strong oral and written communication skills

• This position may require travel up to 25% of the time

Why join us?

Ongoing development is vital to us, you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success.

ICON Plc is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.