Senior Clinical Scientist
hace 3 semanas
As a Senior Clinical Scientist at ICON, you will be part of the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence.
Key Responsibilities:
- Develop and implement medical data review plans to ensure high-quality data for clinical trials.
- Collaborate with cross-functional teams to determine data retrieval strategies and develop study-specific Table of Contents (TOC).
- Provide expert support and suggestions on data processing and analysis to meet compound and study needs.
- Review Safety TFLs and develop Safety Slide Decks for cross-functional review.
- Prepare summaries of safety data reviews, including data reviewed, safety findings, and data cleaning requests.
- Review patient-specific and overall safety data presented in clinical study reports (CSRs).
Requirements:
- Experience in medical data review and clinical trials.
- Data management experience in life sciences/pharmaceuticals.
- Knowledge of regulatory requirements and guidelines.
- Excellent communication and collaboration skills.
What ICON Offers:
- A competitive salary and benefits package.
- A diverse and inclusive work environment.
- Opportunities for professional growth and development.
At ICON, we value diversity, inclusion, and belonging. We are committed to providing an inclusive and accessible environment for all candidates and employees. If you need a reasonable accommodation for any part of the application process, please let us know through our reasonable accommodations form.
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