Senior Clinical Research Scientist
4 weeks ago
As a Senior Clinical Scientist at ICON, you will be part of a world-class team that is dedicated to delivering high-quality clinical research services to the pharmaceutical industry.
Key Responsibilities:- Develop and implement medical data review plans to ensure the accuracy and integrity of clinical trial data.
- Collaborate with cross-functional teams to develop and implement study-specific Table of Contents (TOC) and core TFLs.
- Review Safety TFLs and develop Safety Slide Decks for cross-functional review.
- Query identifiable safety-related medical discrepancies or requests for clarification in the appropriate EDC.
- Prepare summaries of safety data reviews, including data reviewed, safety findings, and data cleaning requests.
- Experience in medical data review and clinical trials.
- Strong data management skills and experience in life science/pharma.
- Experience in one of the following therapeutic areas: cardiovascular/renal, ophthalmology, cell and gene therapy, and oncology.
- 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. If you require a reasonable accommodation for any part of the application process, please let us know through the form below.
Apply now and join our team of talented professionals who are dedicated to delivering high-quality clinical research services.
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