Laboratory For Cancer Risk & Assessment, Cross Cancer Institute Work Values

Daily Duties at Laboratory For Cancer Risk & Assessment, Cross Cancer Institute:

As a Scientific Manager, I coordinated a project in that the drug screening for small molecules of natural plants and proteins was performed to identify useful anti-cancer drugs. The toxic efficiency of these compounds were determined in both in vivo and in vitro, useful drugs were developed the novel anticancer drugs with nanotechnology. As a result, clinical trial Phase I for one novel anticancer drug was completed and is testing in Phase II.

What they like about Laboratory For Cancer Risk & Assessment, Cross Cancer Institute:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

American company, Canadian Company, Toxicology , In vitro & in vivo, Drug development, American/Canadian company, Novel technology development, Experience in GLP, CMC documentation

Skills

Over 12 years of professional designation in toxicology and biological analytical chemistry. studies toxic effects of drugs, environmental toxins on bio-molecules, proteins, cells and biological functions of human, and animals , Plans, designs and conducts studies to measure toxicological effects of toxic substances by using human cells, human tissues and laboratory animals with molecular, biochemical, cellular, animal model and computer model systems., Maintains current knowledge of technical advances of drug toxicology, identifies challenges and opportunities associated with drug toxicology, initiates and plans new toxicological projects, Very familiar with various toxicological technologies, including in vivo/in vitro methods, molecular/cellular/immuno methods and modern instrumentation such as ICP-MS, LC/GC-MS, HPLC, GC, AA, UV, IR, etc., as well as various other analytical technique., Wide exposure to quality control, quality assurance, manufacturing, validation, compliance and regulatory areas in a pharmaceutical manufacturing environment., Writes SOPs and plans toxicological experiments. Executes in vivo and in vitro toxicological, analytical and biological methods to determine toxicity of toxins, validating the methods to meet the regulatory requirements., Collects and maintains experimental data and interprets the data in terms of toxicological effects of substances. Prepares the toxicological data of products to meet regulatory agency requirements and for FDA applications.

These are some of the questions we asked our climbers about their experiences with Laboratory For Cancer Risk & Assessment, Cross Cancer Institute: