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Clinical Research Associate

vor 2 Monaten


Munich, Bayern, Deutschland Allucent Vollzeit
About the Role

We are seeking a highly skilled Sr. Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the smooth execution of clinical trials, from site initiation to close-out.

Key Responsibilities
  • Site Monitoring: Conduct regular site visits to ensure compliance with Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, and study protocols.
  • Regulatory Compliance: Verify and maintain regulatory documents, including informed consent forms, study protocols, and site contracts.
  • Data Management: Track and supervise the collection of study data, ensuring accuracy and completeness.
  • Communication: Serve as the primary point of contact between the project team and site staff, facilitating effective communication and issue resolution.
  • Quality Assurance: Identify and mitigate potential issues, ensuring the integrity of clinical trials.
Requirements
  • Experience: At least 5 years of clinical monitoring experience or relevant clinical trial experience.
  • Education: Relevant life science degree or healthcare background.
  • Skills: Strong communication and interpersonal skills, with the ability to work independently and prioritize tasks effectively.
  • Language: Fluency in English, with strong written and verbal communication skills.
What We Offer
  • Competitive Salary: A comprehensive benefits package, including competitive salaries and flexible working hours.
  • Professional Development: Opportunities for growth and development, including departmental study/training budgets and leadership mentoring.
  • Remote/Hybrid Work: The option to work remotely or in a hybrid environment, depending on location.