Clinical Site Specialist

Vor 5 Tagen


Berlin, Berlin, Deutschland Pharmiweb Vollzeit
Job Summary

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.
Requirements
  • 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.
What We Offer

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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