Site Engagement Liaison

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

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.

We are currently recruiting for an experienced  Senior Clinical Research Associates or Lead CRAs in Romania who are ready to move to another challenge. 

This particular role is a client dedicated one where you will work exclusively on one sponsors trials and SOPs; you will work for a client that values their staff and puts an emphasis on career development. 

In this role your will be  responsible for site monitoring and site engagement activities. 

Responsibilities:

• Maximizing site performance and site engagement in sponsor conducted clinical studies.
• Responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities.
• Engages with clinical sites to develop, build, and maintain strong relationships with investigators/staff that will ensure high quality investigative sites to support sponsor’s clinical development programs.
• Collaborate with internal and external stakeholders as well as third party vendors.
• Responsible for all kinds of site visits (e.g. Selection / Initiation / Monitoring / Close-out / Motivational / Support) and sites’ performance regarding set-up, conduct and data collection
• Primary contact for sites regarding study-related issues.
• Responsible for the early engagement with Key Opinion Leaders (KOLs)/ sites / patients organizations and key contact point for these throughout the study.
• Interact/train new investigators to work on sponsor's clinical trials.
• Attend key therapeutic trainings/meetings and/or industry trainings.
• Provide operational support to the Project Managers to deliver the study within planned timelines and according to required standards of quality and compliance.
• Evaluate, screen and develop high quality investigative sites to support sponsor’s clinical development programs

Requirements:

• A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required
• Previous experience in site engagement or an investigator facing role (e.g. clinical project manager, study director/coordinator, clinical research associate, patient/site engagement companies)
• S., M.S. degree in a life science/biological related field preferred.
• At least 3 years experience in monitoring of trials in clinical development environment,
• Strong Knowledge of GCP and ICH Guidelines.

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, including subsidiaries, 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.

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