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Clinical Reviewer
2 months ago
Position Overview
The FDA's Center for Drug Evaluation and Research (CDER) plays a pivotal role in safeguarding public health by ensuring the safety and efficacy of pharmaceuticals. As a regulatory body, the FDA oversees a wide array of products, including human and animal drugs, medical devices, and biologics, ensuring they meet stringent safety standards.
Mission of the Center for Drug Evaluation and Research
CDER's mission is to enhance public health by ensuring that safe and effective medications are accessible to the population. This includes the regulation of both over-the-counter and prescription drugs, as well as biological therapeutics and generics.
FDA Office of Oncological Disease - Our Commitment
Our team of oncologists and hematologists is dedicated to improving cancer treatment through collaboration with researchers, patients, and global regulatory bodies. We focus on patient-centered regulatory decisions to facilitate the availability of effective therapies for cancer patients.
We maintain our clinical expertise by dedicating time to patient care in various oncology centers. Our affiliations include leading institutions, allowing us to stay at the forefront of clinical practice.
Career Development Opportunities
At the FDA, medical officers have the opportunity to engage in both clinical practice and research. Many of our staff continue to see patients while also contributing to groundbreaking research, publishing in high-impact journals, and participating in expert working groups.
Key Responsibilities
Medical officers at the FDA are tasked with:
- Evaluating the safety and effectiveness of human drugs intended for interstate commerce.
- Ensuring the safety and efficacy of vaccines and biological products.
- Overseeing the safety of medical devices and mitigating unnecessary exposure to radiation.
- Conducting inspections and investigations within the pharmaceutical and food industries.
Qualifications
Applicants should possess an MD or DO from an accredited institution in the United States or Canada. Candidates must be US citizens or Green Card holders and should have a solid understanding of the regulatory aspects of drug development.
