Clinical Research Specialist

2 dagen geleden


Randstad, Nederland Julius Clinical Voltijd

We are seeking a skilled Clinical Research Associate to join our team at Julius Clinical. As a key member of our CRA team, you will be responsible for monitoring clinical research trials in accordance with protocols, SOPs, and applicable laws.

Your primary duties will include:

  • Monitoring clinical research trials, ensuring adherence to protocols, SOPs, and regulatory guidelines;
  • Conducting feasibility assessments, site selection, initiation, monitoring, and close-out visits;
  • Evaluating the quality and integrity of study site practices;
  • Managing the progress of assigned studies, including tracking regulatory submissions, recruitment, and data query resolution;
  • Developing and maintaining effective working relationships with site staff and investigators;
  • Create and maintain accurate documentation regarding site management and monitoring visit findings.

In addition to your technical skills and experience, you should possess excellent communication and negotiation skills, as well as the ability to work independently in a team-oriented environment.

We offer a dynamic and innovative work environment, opportunities for professional growth and development, and a competitive compensation package.



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