Clinical Site Manager

Vor 6 Tagen


Munich, Bayern, Deutschland Pharmiweb Vollzeit
Clinical Site Manager Job Description

As a Clinical Site Manager at ICON plc, you will be responsible for 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.

Our company, ICON 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.

Key Responsibilities:

  • Plan, initiate, coordinate, and manage 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 our 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 our clinical development programs.
  • Engage with Key Opinion Leaders (KOLs)/sites/patients organizations and serve as the key contact point for these throughout the study.
  • Interact/train new investigators to work on our clinical trials.
  • Attend key therapeutic trainings/meetings and/or industry trainings.

Requirements:

  • 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.

What ICON Can Offer You:

Our success depends on the quality of our people. 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 benefits, including various annual leave entitlements, health insurance offerings, competitive retirement planning, and a global Employee Assistance Programme.

Visit our careers website to learn more about the benefits of working at ICON: https://careers.iconplc.com/benefits

ICON is an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment.



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