Clinical Research Associate II

4 weken geleden


Amsterdam, Noord-Holland, Nederland Allucent Voltijd
About the Role

We are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a Clinical Research Associate II, you will play a critical role in the success of our clinical trials by ensuring that all study-related activities are conducted in accordance with Good Clinical Practice (GCP) and applicable regulations.

Key Responsibilities
  • Conduct site visits to monitor the progress of clinical trials and ensure compliance with study protocols and regulations.
  • Review and verify study-related documents, including informed consent forms, case report forms, and study protocols.
  • Collaborate with site staff to resolve any issues or concerns that may arise during the conduct of the study.
  • Prepare and submit study-related reports, including site visit reports and study close-out reports.
  • Participate in the development and implementation of study protocols and procedures.
Requirements
  • At least 2 years of experience in clinical research, preferably in a regulatory or compliance role.
  • Strong knowledge of GCP and applicable regulations, including ICH and FDA guidelines.
  • Excellent communication and interpersonal skills, with the ability to work effectively with site staff and other stakeholders.
  • Ability to work independently and as part of a team, with a strong attention to detail and organizational skills.
What We Offer
  • A competitive salary and benefits package.
  • The opportunity to work with a dynamic and growing company.
  • A collaborative and supportive work environment.
  • Professional development opportunities, including training and mentorship.


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