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Understand the broader ADME requirements of various projects
Have expert understanding of the different approaches related to preclinical pharmacokinetics, as well as a good understanding of related disciplines (e.g., toxicokinetics, nonclinical safety, PKPD, PK modelling, drug design, clinical DMPK, bioanalytics and biomarkers)
Design DMPK strategy and implementation plan
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
Must demonstrate excellent verbal and technical communication, independent scientific thinking, with the ability to interpret results, determine next steps and present data to project teams and senior management.
Design tailor made IN VIVO PK protocols for various projects
Collate the obtained results and prepare presentations for internal and external meetings with clients (FFS/DD projects)
Prediction of human pharmacokinetic properties from in vitro and in vivo data
Data generation, compilation, report preparation, record keeping, SOP writing
Management towards optimising utilization of lab resources
Manage animal house and laboratory instruments properly.
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Date Posted: 26/07/2024
Job ID: 86507873
