Clinical Research Associate
hace 2 semanas
Clinical Research Associates are vital to the success of our Sponsor dedicated team at IQVIA. As a junior CRA, you will be responsible for performing site selection, initiation, monitoring, and close-out visits.
Your Responsibilities:- Conduct thorough site assessments to ensure compliance with regulatory requirements
- Support the development of subject recruitment plans to optimize study outcomes
- Evaluate the quality and integrity of site practices, adhering to Good Clinical Practice and International Conference on Harmonization guidelines
- Manage progress by tracking regulatory submissions, case report form completion, and data query resolutions
- Collaborate with experts at study sites and client representatives to achieve study objectives
To succeed in this role, you will need:
- A university degree in a scientific discipline or healthcare
- Experience in the Pharma Industry or Clinical Trials environment
- Excellent computer skills, including MS Office
- Proficiency in Spanish and English language
- Strong organizational, time management, and problem-solving skills
- The ability to establish and maintain effective working relationships
- Flexibility to travel and hold a valid driver's license class B
We provide:
- A comprehensive benefits package, including company car and mobile phone
- A stable, international work environment with opportunities for career growth
- A flexible work schedule and supportive leaders
- Resources to build your therapeutic knowledge and expertise
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We strive to create a healthier world by pushing the boundaries of human science and data science.
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