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| Job Location | London |
| Education | Not Mentioned |
| Salary | £22,000 - £23,000 per annum, negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
*Salary currently confidential - Please apply or get in contact for details*Location - Home-working from within the UK.This is a global professional services provider offering research, analytics, and data management services. They are powered by mind+machine - a unique combination of human expertise and best-in-class technologies that use smart algorithms to simplify key tasks. They work with clients across a wide range of industries and business functions, helping them to make better decisions faster; reach new levels of efficiency and effectiveness; and see a tangible impact on their top and bottom line.This is a highly technical specialist role, you must have a high level of understanding of chemical regulations (laws constantly changing, environmental impacts etc). This role has been created to due strong growth in the area, there is a lot of exciting work coming in for this company - this is a big area for consumer good companies (FMCG, tech, etc.)Job description:• To provide evidence of efficacy and safety (preclinical and clinical) as per regulatory requirements• Scientific literature search -To extract, analyze and collate toxicology data from various clinical/toxicology/efficacy related databases like TOXNET, HSDB, PubMed, Medline, ScienceDirect etc.• To evaluate quality of different toxicity studies (such as systemic toxicity, genotoxicity, skin/eye irritation, sensitization, carcinogenicity, reprotoxicity and developmental, toxicokinetics studies) as per OECD/ ICH /FDA guidelines• To identify, evaluate and summarize critical toxicology data for drafting hazard or safety assessment on a chemical (pharmaceuticals/ cosmetics/ nutraceuticals/ agrochemicals/ botanicals/ biomedical devices).• To prepare research reports/ dossiers according to the international regulatory guidelines• To draft environmental assessment for various chemicals with respect to persistence bioaccumulation and toxicity.Skills needed:• M. Pharm./M.S. (Pharm.) in Pharmacology/Toxicology/Regulatory Toxicology• 2-6 years research experience in pharmaceutical industry/CRO’s (preferably in pre-clinical toxicity studies/toxicology projects)• Thorough understanding of various toxicological studies and their principles• Capability of interpretation of results and analysis of key toxicity data.• Knowledge of OECD/FDA/EPA guidelines for preclinical toxicity studies• Knowledge of various toxicology/ pharmacology/ clinical/ regulatory databases like TOXNET, ECOTOX, PubMed, e-Chemportal, clinicaltrails.gov, EFSA etc.• Basic knowledge of clinical trials• Basic knowledge of eco/environmental toxicity (e.g. biodegradation, toxicity to daphnia, fish (acute and chronic), toxicity to algae)• Knowledge of dose calculation/conversion• Act as an efficient team player with good reasoning.• Ability to identify pro-active ways to contribute to firms goals & mission• Challenging current thinking by implementing new ways of working Required skills
Keyskills :
Research Toxicology