Clinical Site Specialist
Vor 5 Tagen
We are seeking a skilled Clinical Site Manager to join our team at ICON. As a Clinical Site Manager, you will be responsible for maximizing site performance and engagement in our client-conducted clinical studies.
Key Responsibilities- Site Performance and Engagement: Develop and implement strategies to maximize site performance and engagement in clinical studies.
- Site Management: Supervise and coordinate site-related activities to ensure compliance with client Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and regulatory requirements.
- Site Development: Evaluate, screen, and develop high-quality investigative sites to support our client's clinical development programs.
- Collaboration and Communication: Collaborate with internal and external stakeholders, including investigators, site staff, and third-party vendors, to ensure successful study execution.
- Qualifications: SCRA with a minimum of 4+ years of monitoring experience in Germany.
- Language Skills: Excellent verbal and written communication in German and English.
- Operational Skills: Ability to operate effectively within an international and rapidly changing environment.
- Supervisory Skills: Ability to supervise monitoring and related activities in a clinical trial.
- Scientific Knowledge: Ability to have scientific discussions with Investigators and Site Personnel.
At ICON, we are committed to creating a diverse and inclusive workplace that rewards high performance and nurtures talent. Our benefits include competitive salaries, annual leave entitlements, health insurance, retirement planning, and more.
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