Clinical Research Associate

vor 3 Wochen


Munich, Bayern, Deutschland Allucent Vollzeit
Job Description

We are seeking a highly skilled Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for monitoring and managing clinical trials to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

Key Responsibilities
  • Site Monitoring: Conduct on-site visits to investigate sites, monitor trial activities, and ensure compliance with study protocols and regulations.
  • Regulatory Compliance: Ensure that all trial-related documents and records are accurate, complete, and compliant with regulatory requirements.
  • Communication: Serve as the primary point of contact between the project team and site staff, ensuring effective communication and issue resolution.
  • Quality Assurance: Identify and report quality issues, and participate in the development and implementation of corrective and preventive actions.
Requirements
  • Experience: At least 5 years of clinical monitoring experience, with a strong background in GCP and regulatory compliance.
  • Education: Relevant life science degree or healthcare background, with a strong understanding of medical terminology and clinical monitoring processes.
  • Skills: Strong communication and interpersonal skills, with the ability to work independently and as part of a team.
  • Language: Fluency in English, with the ability to communicate effectively in a global environment.
Benefits
  • Competitive Salary: A comprehensive benefits package, including a competitive salary and opportunities for professional growth and development.
  • Flexible Working Hours: Flexible working hours, with the option to work remotely or in a hybrid environment.
  • Leadership Opportunities: Opportunities for leadership and mentoring, with a focus on career development and advancement.


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