Clinical Site Manager

As Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well as leveraging strong clinical operational and therapeutic expertise (scientific, clinical, disease states, and treatment alternatives knowledge within the therapeutic area(s)) to support execution of the clinical studies.

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.

Responsibilities:

• Responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with the client Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory requirements
• Engage with clinical sites to develop, build, and maintain strong relationships with investigators/staff that will ensure high quality investigative sites to support the client’s clinical development programs
• Collaborate with internal and external stakeholders as well as third party vendors
• Provide operational support to the CPM/Sr CPM 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 the client’s clinical development programs
• 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 the client clinical trials
• Attend key therapeutic trainings/meetings and/or industry trainings

To be successful in the role, you will have:

• A SCRA with a minimum of 4+ years of monitoring experience in Germany 
• Excellent verbal and written communication in German and English
• Operate effectively within an international and rapidly changing environment

• Please note that this is a traveling position and you will have to be willing to travel at least 50% of the time (including overnight stays)

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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