Lavori attuali relativi a Clinical Research Associate, Site Management Specialist - Milano, Lombardia - IQVIA
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Clinical Research Associate, Site Management Specialist
2 mesi fa
As a Clinical Research Associate at IQVIA, you will play a critical role in ensuring the success of clinical trials by conducting site monitoring visits and providing training to study sites.
**Key Responsibilities:**
* Conduct site monitoring visits to ensure compliance with study protocols and regulatory requirements
* Provide training to study sites on clinical research procedures and Good Clinical Practice (GCP) guidelines
* Evaluate the quality and integrity of study site practices and escalate quality issues as necessary
* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution
* Collaborate with study team members to ensure project execution support
**Requirements:**
* Bachelor's degree in a scientific discipline or healthcare preferred
* Equivalent combination of education, training, and experience may be accepted in lieu of degree
* Prior clinical experience preferred
* Advanced knowledge of applicable clinical research regulatory requirements, including GCP and ICH guidelines
* Strong organizational and problem-solving skills
* Effective time and financial management skills
* Ability to establish and maintain effective working relationships with coworkers, managers, and clients
**About IQVIA:**
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.
If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity to join our team at IQVIA.
