Senior Safety Associate
2 days ago
The Senior Safety Associate will be responsible for ensuring the timely and accurate collection, processing, and tracking of serious adverse event (SAE) reports.
This involves working closely with cross-functional teams to generate safety narratives and queries, perform quality control of safety cases, and prepare clinical safety documents.
Key Responsibilities- Manage the processing of SAE reports, ensuring compliance with regulatory requirements.
- Collaborate with the clinical trial team to develop and implement safety protocols.
- Conduct quality control reviews of safety cases and generate Investigator Safety Letters as required.
- Support the preparation of clinical safety documents, including TMF uploads and quality control reviews.
- Participate in internal and external meetings to discuss clinical trial progress and safety concerns.
- Lead clinical trial projects, ensuring timely completion and adherence to regulatory guidelines.
Competitive Salary: $70,000 - $90,000 per annum.
About Our CompanyWe are a leading CRO, dedicated to accelerating the development of safe and effective medical therapeutics through our scientific approach.
With expertise in oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective areas, we provide comprehensive clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Our team of experts works collaboratively to deliver high-quality results, ensuring client satisfaction and success.
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