Our global reach, recognized scientific leadership and expertise in drug development makes Covance well positioned to support pharmaceutical and biotechnology companies. Working from the leading edge, our industry-leading preclinical and central laboratory testing platforms and our extensive experience in clinical trials strategically positions us and our employee stockholders for growth.

Join us in any of these areas to move new medical therapies through development, and ultimately, to the patient.

Career Options in Early Development Services

Our expertise in toxicology, phase I, research products, drug metabolism, and pharmacokinetics helps clients maximize the chances of success in the clinical phases. We offer comprehensive services in all these areas with a thorough understanding of the regulatory, scientific, and commercial environments. Covance has commenced a major expansion of our toxicology facilities around the world. This additional space will significantly increase our preclinical capacity globally.

Our global bioanalytical service focuses on high efficiency testing on all stages of development. Covance is the only CRO that can provide both bioanalytical and central laboratory services on a large scale. The addition of these capabilities makes us an even more valuable resource for our clients.

Career Options in Late Stage Development

Our late stage services are made up of Covance’s ability to offer clients phase II through IV clinical trials and post-marketing services. Our global capabilities include having scientists and managers worldwide who are experts in clinical development and support services, periapproval strategies, and health economics and outcomes. Covance can conduct clinical trials professionally and economically almost anywhere in the world. Taking control of logistical costs by eliminating patient over-enrollment, minimizing drug supply wastage, and transforming electronic patient diaries into decision-making tools is possible using our interactive voice response (IVR) technology. Additionally, our depth of expertise and experience allows us to align the clinical and financial incentives for providers to prescribe, payers to cover, and patients to use new medical products and technologies.

As the industry leader in central laboratory services, we are poised for growth in a billion dollar marketplace. With a focus on automation and applied sciences, we link our scientific experience with state-of-the-art technology for DNA ad RNA extraction, alliquoting and banking. We also provide real-time access to genetic assays and pathway analysis. Covance offers a sophisticated and complex total system to complete clinical trial ECGs in a digital environment that is already compliant with the new standards proposed by the FDA. In fact, we further advanced our leadership by obtaining certification as compliant with ISO 9001, a globally recognized gold standard for QA.

Our global capacity reaches the Americas, UK, Europe, and Asia Pacific. With our success in becoming the partner of choice in drug development, what better choice could you make then to join us in one of many career options we’re offering now!