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Clinical Research Associate

vor 2 Monaten


Munich, Bayern, Deutschland SciPro Vollzeit

Job Summary:

Clinical Research Associate (CRA) at SciPro

About the Role:

We are seeking a highly skilled Clinical Research Associate to join our team at SciPro. As a CRA, you will play a critical role in the success of our clinical trials by ensuring compliance with regulatory requirements and industry standards.

Key Responsibilities:

  • Conduct on-site monitoring visits to trial sites to ensure compliance with Good Clinical Practice (GCP) and regulatory requirements
  • Review and verify trial site documentation, including informed consent forms, case report forms, and study protocols
  • Collaborate with trial site staff to resolve any issues or concerns related to the trial
  • Prepare and submit monitoring reports to the sponsor
  • Participate in the development and implementation of clinical study protocols and procedures

Requirements:

  • Bachelor's degree in a life science or a related field
  • Minimum 2 years of experience in clinical research, preferably as a CRA
  • Strong knowledge of GCP, regulatory requirements, and industry standards
  • Excellent communication and interpersonal skills
  • Ability to work independently and as part of a team

What We Offer:

SciPro offers a competitive salary and benefits package, as well as opportunities for professional growth and development.