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Regulatory Specialist for Clinical Research Start-ups

hace 2 meses


Barcelona, Barcelona, España IQVIA A tiempo completo
Key Qualifications

We are seeking a highly skilled Regulatory Start-up/Site Activation Specialist to join our team at IQVIA. The ideal candidate will possess a Bachelor's Degree in a related field and a minimum of 2 years of clinical research experience.

  • Education and Experience: Bachelor's Degree in a related field and 2 years of clinical research experience or an equivalent combination of education, training, and experience.
  • Clinical Systems and Procedures: In-depth knowledge of clinical systems, procedures, and corporate standards.
  • Medical Terminology and Regulations: Strong knowledge of medical terminology and regulations.
  • Clinical Research Knowledge: Broad knowledge of clinical research.
  • Technical Skills: Strong knowledge of Microsoft Office and e-mail applications.
  • Soft Skills: Effective communication, organizational, and interpersonal skills.
  • Project Management: Ability to work independently and effectively prioritize tasks, manage multiple projects, and establish and maintain effective working relationships with coworkers, managers, and clients.

We offer a dynamic and challenging work environment that will allow you to grow and develop your skills. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.