Clinical Research Associate

1 week geleden


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

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 investigational sites to ensure the successful execution of clinical trials.

Key Responsibilities
  • Independently monitor and manage investigational sites to ensure compliance with Good Clinical Practices (GCP) and applicable regulations.
  • Conduct site visits to assess site performance and provide guidance to site staff as needed.
  • Develop and maintain strong relationships with site staff, investigators, and sponsors to ensure effective communication and collaboration.
  • Identify and mitigate potential risks and issues related to site management and clinical trial execution.
  • Prepare and submit high-quality site visit reports and contact reports in a timely manner.
Requirements
  • At least five years of clinical monitoring experience and/or relevant clinical trial experience.
  • Relevant life science degree or medical/nursing background, or combination of education and experience.
  • Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures.
  • Strong written and verbal communication skills, including good command of English and local language.
  • Ability to work in a fast-paced, dynamic environment and adapt to changing priorities and deadlines.
What We Offer
  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • Collaborative and dynamic work environment.
  • Flexible working hours and remote work options.


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