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2 days ago
This Clinical Research Associate position at IQVIA Turkey involves conducting site visits, evaluating site practices, and developing subject recruitment plans. As a CRA, you will play a crucial role in ensuring the quality and integrity of our clinical trials.
Key Responsibilities:
- Perform site visits to assess compliance with regulatory requirements.
- Develop and implement subject recruitment strategies.
- Evaluate site practices and provide recommendations for improvement.
- Collaborate with site staff and clients to achieve project goals.
Requirements:
- University degree in a relevant field.
- Relevant experience in the Pharma industry or clinical trials.
- Strong analytical and problem-solving skills.
- Excellent communication and collaboration skills.
- Flexibility to adapt to changing priorities.
About IQVIA:
We are a global leader in clinical research services, commercial insights, and healthcare intelligence. Our goal is to improve patient outcomes by accelerating the development and commercialization of innovative medical treatments.
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