Ref #: 32216

Employment type: Permanent - Full-Time

Location: Israel

Posted: 21-Sep-2021


ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre 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.

•Management Clinical Trials according to the protocol and ICH GCP, standard operation procedures and monitoring plan.
•Knowledge and understanding of the protocol and CRF content
•Keeping contact with the Investigator.
•Supporting sites with all issues concerning study.
•Providing information to investigators about: protocol principles, study timelines, enrolment expectations and proposed fee.
•Preparing and performing Initiation Visit and Monitoring Visit according to the GCP and monitoring plan.
•Preparing Institution and Investigator fees documentation.

What is required:
•A life science / healthcare related degree or equivalent work experience.
•Minimum 2-3 years of study coordinator experience or experience as in-house CRA or CRA (min. 6 months)
•Solid understanding of clinical trial design, trial execution and operations.
•Knowledge of international standards (GCP/ICH), international (FDA, EMEA) and local regulations.
•Expertise in communication, managing multiple priorities and computer literacy.
•Proven people management skills with demonstrated expertise in working in a team.
•Fluency in English as well as Polish.
•Availability to travel at least 60% fly and drive and should possess a valid driving license.

What is offered:
•A challenging CRA role in an international Pharmaceutical company.
•Permanent office based position in a stable organization.
•You will enjoy highly competitive compensation and an exceptional benefits package.

Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.