Clinical Research Associate Specialist

hace 4 semanas


Barcelona, Barcelona, España Pharmiweb A tiempo completo

Clinical Trials Coordinator

Transforming Clinical Development: A New Era in Scientific Rigor

At Pharmiweb, we're committed to revolutionizing the clinical development process by ensuring the swift delivery of life-changing ideas and therapies to patients in need. As a Clinical Trials Coordinator, you'll play a pivotal role in shaping the future of clinical research.

Key Responsibilities:

  • Implement clinical monitoring procedures in accordance with ICH GCP Guidelines and local regulatory requirements.
  • Conduct site monitoring responsibilities for clinical trials, ensuring the protection of subjects and data integrity.
  • Prepare and implement project plans related to Clinical Monitoring responsibilities, guaranteeing audit readiness at site level.
  • Collaborate with the study team to ensure study deliverables are met, and assist with the administration of clinical research projects.

Qualifications:
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution.
  • Thorough understanding of ICH GCP Guidelines and local regulatory requirements.
  • Fluent in local office language and in English, both written and verbal.

Benefits:
  • Opportunity to work in a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
  • Chance to be part of a team that's passionate about overcoming barriers in clinical trials.

About Us:
Pharmiweb is an Equal Opportunity Employer, committed to diversity and inclusion in the workforce. We strive for a workplace where all employees feel valued, respected, and empowered to contribute their best work. Join us in our mission to transform clinical development and make a difference in the lives of patients worldwide.

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