Clinical Site Manager
vor 2 Wochen
As a Clinical Site Manager, you will play a crucial role in maximizing site performance and engagement in our client-conducted clinical studies. You will leverage your strong clinical operational and therapeutic expertise to support the execution of clinical studies.
About ICON plcICON plc is a world-leading healthcare intelligence and clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations. Our patients are at the center of all that we do, and we help accelerate the development of drugs and devices that save lives and improve quality of life.
Key Responsibilities:- Plan, initiate, coordinate, and manage all monitoring and monitoring-related activities, ensuring compliance with 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, ensuring high-quality investigative sites to support client 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 client clinical development programs.
- Responsible for 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 client clinical trials.
- Attend key therapeutic trainings/meetings and/or industry trainings.
- SCRA with a minimum of 4+ years of monitoring experience in Germany.
- Excellent verbal and written communication in German and English.
- Ability to 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.
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits, including various annual leave entitlements, health insurance offerings, competitive retirement planning, and more.
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
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 or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
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