Clinical Research Associate II

vor 4 Wochen


Munich, Bayern, Deutschland Pharmiweb Vollzeit
Job Summary

As a Clinical Research Associate II in Germany, you will be part of a dynamic team responsible for the conduct of clinical trials. Your primary focus will be on monitoring and managing clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

Key Responsibilities
  • Conduct site initiation visits, monitor study progress, and ensure compliance with study protocols and regulations.
  • Collect and manage clinical trial data, including source documents and case report forms.
  • Collaborate with cross-functional teams, including study managers, data managers, and biostatisticians, to ensure trial success.
  • Identify and mitigate risks, and implement corrective actions as needed.
  • Develop and maintain strong relationships with site personnel, investigators, and other stakeholders.

Requirements
  • 18 months+ of monitoring experience in phase I-III trials as a CRA.
  • College degree in medicine, science, or equivalent.
  • Previous monitoring experience in medium-sized studies, including study start-up and close-out.
  • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.
  • Excellent written and verbal communication in German and English.
  • Ability to work to tight deadlines and travel extensively (at least 60% of the time).

What We Offer

At ICON, we value our employees and offer a range of benefits to support their well-being and career development. These include competitive salaries, annual leave entitlements, health insurance, retirement planning, and flexible work arrangements. We also offer opportunities for professional growth and development, including training and mentoring programs. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.

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