Jubilant Biosys Ltd Pharma Job Opening 2022 – Apply Online
Jubilant Biosys Ltd Hiring Pharma candidates for the post of Research Associate. Research Associate job opening 2022. Pharma job opening 2022. M Pharma job opening 2022. Pharmacy job 2022. Intrested and eligible candidates may check out all the details on the same below:
Job Title: Research Associate with good experience in Metabolite Identification (Met ID)
Department: DMPK
Eligibility Criteria/ Experience: M.Pharm with 2-6 yrs of expertise in Bioanalysis using LC-MS/MS under GLP and non-GLP environments, quantitation of small molecules using LC-MS/MS and can perform metabolite identification work on High-resolution mass spectrometry.
Key Responsibilities:
- Responsible for drug metabolism and pharmacokinetic support for discovery programs.
Support preclinical bioanalysis - Monitor Pharmacokinetics studies and support bioanalysis
- Providing pre-clinical ADME lead optimization support to small molecule Drug Discovery programs (Hit Identification to Clinical Candidate Selection) including Inflammation,
- Neuroscience, Metabolic Disorders and Anti-infective Research.
- Understand the Chemical Structure – ADME relationships and design apt strategies for improving Drug-like Properties of the New Chemical Entities.
- Understand the broader ADME requirements of various projects
- Conduct PK and PK/PD analysis through early pre-clinical development, and collaborate in PK/PD and efficacy study designs
- Collaborate with safety assessment group (in need basis) on study design
- Design tailor-made ADME protocols for various projects
- Collate the obtained results and prepare presentations for internal and external meetings
- Contribute to the design of the critical path for various projects
- Prediction of human pharmacokinetic properties from in vitro and in vivo data
- Managing PK and PK/PD analysis through early pre-clinical development, and collaborating in PK/PD and efficacy study design developing robust PK/PD models
- Prediction of human pharmacokinetic properties from in vitro and in vivo data in preclinical species.
- Collaborates with safety assessment group on study design.
- Method validations and analytical troubleshooting; Data generation, compilation, report preparation; Lab notebook, record keeping; SOP writing
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