Clinical Site Manager

at  Icon plc

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
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.

QUALIFICATIONS:

• 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
• Ability to supervise monitoring and related activities in a clinical trial
• Ability to have scientific discussions with Investigators and Site Personnel
• BA/BS Degree required
• Ability to travel domestically

• 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