Regulatory Specialist
hace 2 semanas
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
Key Responsibilities:- Qualifications: Bachelor's Degree in a related field and 2 years of clinical research experience or 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: Broad knowledge of clinical research.
- Technical Skills: Strong knowledge of Microsoft Office and e-mail applications.
- Communication and Interpersonal Skills: Effective communication, organizational, and interpersonal skills.
- Project Management: Ability to work independently and to effectively prioritize tasks, manage multiple projects, and establish and maintain effective working relationships with coworkers, managers, and clients.
We are seeking a highly skilled Regulatory Start-up/Site Activation Specialist to join our team in Spain. As a key member of our team, you will be responsible for ensuring the successful start-up and activation of clinical research sites.
If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.
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