CRA II

As a top 5 CRO in the world, we are looking to strengthen our Clinical Operations team in Turkey. We empower our CRA's to work independently and enthusiastically to balance all necessary activities required.

As a CRA at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

Overview of the Role

·         Independent, proactive work to set up and monitor studies, complete reports and maintain documentation

·         Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions

·         Balancing sponsor generated queries

·         Taking responsibility for study cost efficiency

·         Preparation and review of study documentation and feasibility studies for new proposals

·         Potential to assist in training and mentoring fellow CRAs

Role Requirements

·         University degree in medicine, science, or equivalent

·         Previous monitoring experience in medium-sized studies, including study start-up and close-out

·         Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data

·         Excellent written and verbal communication in English and Turkish

·         Ability to work to tight deadlines

·         Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license

Benefits of Working at ICON

Other than working with an outstanding team of ambitious people, we also offer a very competitive compensation package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

Following your application, you will be contacted by one of our dedicated recruiters and if successful, we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - M/F/D/V and committed to delivering a workplace free of any discrimination or harassment.

EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origin