Clinical Research Associate
1 miesiąc temu
Drive healthcare innovation by joining our team of skilled Clinical Research Associates at IQVIA.
Key Responsibilities
- Conduct site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Collaborate with sites to adapt and track subject recruitment plans, enhancing predictability.
- Administer protocol training to assigned sites and establish regular communication to manage ongoing project expectations.
- Evaluate study site practices and escalate quality issues as necessary.
- Manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
- Maintain accurate documentation of site management, monitoring visit findings, and action plans.
Requirements
- Life science degree education.
- Independent on-site monitoring experience.
- Experience handling multiple protocols and sites across various drug indications.
- Flexibility and ability to travel.
- Strong communication, written, and presentation skills.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We aim to make a significant impact by driving innovation and pushing the boundaries of human science and data science to create a healthier world.
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