You will be responsible for providing drug metabolism and pharmacokinetic support for discovery programs. Your main duties will include monitoring Pharmacokinetics studies, supporting bioanalysis, and offering pre-clinical ADME lead optimization support to small molecule Drug Discovery programs across various therapeutic areas. You will be working as a DMPK subject matter lead in multidisciplinary/cross-functional teams to understand the Chemical Structure ADME relationships and design appropriate strategies to enhance the Drug like Properties of the New Chemical Entities. To be successful in this role, you should have 2-5 years of experience in GLP with either an M.Sc. or Ph.D. degree. You should possess expertise in Bioanalysis using LC-MS/MS in both GLP and non-GLP environments. Additionally, you should be capable of leading projects as a DMPK representative, quantifying small molecules using LC-MS/MS, and conducting metabolite identification work on High-resolution mass spectrometry. Qualifications required for this position include an M. Pharm (Pharmacology / Pharmaceutical Analysis) or an M.Sc. (Biochemistry / Pharmaceutical Chemistry).,
As a Regulatory Toxicology & Pharmacology professional in Kolkata, you will be expected to have a clear understanding of Regulatory Toxicology & Pharmacology principles with robust domain knowledge. Additionally, you should possess a good understanding of OECD guidelines Safety Guidelines and be familiar with risk assessment, Hazard assessment, Exposure assessment & Safety assessment. Your role will also require knowledge of various Toxicology/ Pharmacology/ clinical/ Regulatory databases and dose calculation & conversions. With 2-3 years of experience, you should have the capability of interpretation of results and analysis of key toxicity data. Qualifications required for this position include an M. Pharm in Pharmacy or MS/M.Sc(Science) in Chemistry. Kindly note that there are no additional details about the company provided in the job description.,
You will be responsible for providing drug metabolism and pharmacokinetic support for discovery programs. Your duties will include monitoring Pharmacokinetics studies, supporting bioanalysis, and offering pre-clinical ADME lead optimization support to small molecule Drug Discovery programs. This support will range from Hit Identification to Clinical Candidate Selection in areas such as Inflammation, Neuroscience, Metabolic Disorders, and Anti-infective Research. As a DMPK subject matter lead, you will collaborate in multidisciplinary/cross-functional teams to understand Chemical Structure-ADME relationships and design strategies to enhance Drug like Properties of New Chemical Entities. Key Responsibilities: - Provide drug metabolism and pharmacokinetic support for discovery programs - Monitor Pharmacokinetics studies and support bioanalysis - Offer pre-clinical ADME lead optimization support to small molecule Drug Discovery programs - Collaborate in multidisciplinary/cross-functional teams to enhance Drug like Properties of New Chemical Entities Qualifications: - M. Pharm in Pharmacology or Pharmaceutical Analysis - M.Sc. in Biochemistry or Pharmaceutical Chemistry Please note that the company details were not provided in the job description.,