Clinical Site Management Lead
2 weeks ago
Clinical Site Management Overview: As a Clinical Site Management Lead at ICON plc, you will be responsible for maximizing site performance and engagement in clinical studies. This role requires a high level of clinical operational and therapeutic expertise to support study execution.
\We are a world-leading healthcare intelligence and clinical research organization advancing clinical research with outsourced services to pharmaceutical, biotechnology, medical device, and government organizations. Our patients are at the center of our work, accelerating the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, driving our success with a culture built around collaboration and innovation.
\Key Responsibilities:
- Plan, initiate, coordinate, and manage monitoring and monitoring-related activities, ensuring compliance with client SOPs, GCP, and regulatory requirements.
- Develop strong relationships with investigators and staff to ensure high-quality investigative sites support client clinical development programs.
- Collaborate with internal and external stakeholders, including third-party vendors.
- Provide operational support to deliver studies within planned timelines and according to required quality and compliance standards.
- Evaluate, screen, and develop high-quality investigative sites to support client clinical development programs.
- Engage with Key Opinion Leaders, sites, patient organizations, and key contact points throughout the study.
- Train new investigators on client clinical trials and attend key therapeutic trainings and industry meetings.
Requirements and Qualifications:
\- Requires a SCRA with at least 4+ years of monitoring experience in Germany.
- Excellent German and English verbal and written communication skills.
- Ability to operate effectively in an international and rapidly changing environment.
- Ability to supervise monitoring and related activities in clinical trials and have scientific discussions with Investigators and Site Personnel.
- Requires a BA/BS degree.
- Ability to travel domestically.
Salary and Benefits:
\The estimated salary for this role is €90,000 per year. In addition to a competitive salary, we offer a range of benefits, including annual leave entitlements, health insurance, retirement planning, and flexible country-specific benefits.
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