Multi-Sponsor CRA Role with Excellent Work-Life Balance

vor 1 Woche


Berlin, Berlin, Deutschland Meet Vollzeit

Job Summary:

Meet is seeking a highly skilled Clinical Research Associate/CRA II to join our team in a homebased opportunity. As a CRA II, you will be responsible for performing clinical study site management/monitoring activities in compliance with ICH-GCP and Sponsor SOPs.

Key Responsibilities:

  • Perform site initiation, monitoring, and close-out visits in accordance with ICH-GCP and Sponsor SOPs.
  • Ensure compliance with regulatory documentation for study start-up, maintenance, and close-out.
  • Develop and maintain strong relationships with site personnel and sponsors.
  • Collaborate with cross-functional teams to ensure timely and successful study execution.
  • Identify and report any site-related issues or concerns to the project team.

Requirements:

  • Strong understanding of clinical research and regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Strong problem-solving and analytical skills.
  • Proficiency in Microsoft Office and clinical trial management systems.

What We Offer:

  • Competitive salary and bonus structure.
  • Opportunities for career growth and professional development.
  • Flexible work arrangements, including homebased work options.
  • Collaborative and dynamic work environment.


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