Senior Research Associate at Viiv Healthcare Group of Companies United Kingdom
london, London - England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

05 Feb, 27

Salary

45000.0

Posted On

07 Nov, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

·      Spearhead ADME (Absorption, Distribution, Metabolism, Excretion) studies to support early-stage drug discovery projects.

·      Develop and optimise in-vitro assays, including metabolic stability, enzyme phenotyping, and drug-drug interaction studies.

·      Conduct high-throughput screening using liver microsomes, S9 fractions, and recombinant CYPs for compound profiling.

·      Analyse pharmacokinetic parameters (NCA) and provide actionable insights for candidate selection.

·      Develop and optimise LC-MS/MS methods for the quantification of small molecules and metabolites.

·      Maintain rigorous documentation and compliance with GLP standards.

·      Conducted rodent and non-rodent pharmacokinetic studies, supporting in vitro-to-in vivo translation (IVIVC) for early candidate selection.

·      Validated and developed time-dependent inhibition (TDI) assays (IC₅ shift method), glucuronidation and sulfation studies using S9 fractions and microsomes, contributing to expanded laboratory capabilities.


Responsibilities

·      Spearhead ADME (Absorption, Distribution, Metabolism, Excretion) studies to support early-stage drug discovery projects.

·      Develop and optimise in-vitro assays, including metabolic stability, enzyme phenotyping, and drug-drug interaction studies.

·      Conduct high-throughput screening using liver microsomes, S9 fractions, and recombinant CYPs for compound profiling.

·      Analyse pharmacokinetic parameters (NCA) and provide actionable insights for candidate selection.

·      Develop and optimise LC-MS/MS methods for the quantification of small molecules and metabolites.

·      Maintain rigorous documentation and compliance with GLP standards.

·      Conducted rodent and non-rodent pharmacokinetic studies, supporting in vitro-to-in vivo translation (IVIVC) for early candidate selection.

·      Validated and developed time-dependent inhibition (TDI) assays (IC₅ shift method), glucuronidation and sulfation studies using S9 fractions and microsomes, contributing to expanded laboratory capabilities.


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