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6.0 - 9.0 years
6 - 10 Lacs
Bengaluru
Work from Office
Preferred candidate profile M. Pharm (Pharmacology) / M.Sc. (Biochemistry / Pharmaceutical Chemistry) with 6-9 years or Ph.D. with 2-5 years' experience in PBPK & PK/PD modelling & Gastro plus; Simcyp software Role & responsibilities Experience in the development and application of pharmacometric models to support drug development and regulatory submissions Extensive experience with non-linear mixed effects modelling Proficient with software tools like PBPK models, Phoenix, R, PoPK, QSP modelling or similar platforms Strong background in pharmacokinetics/pharmacodynamics (PK/PD) modelling, First-in-human dose predictions. Collaborate with clinical pharmacology, biostatistics, and other interdisciplinary teams to inform clinical trial designs and data analysis Develop and implement model-based strategies to optimize dosing regimens and therapeutic outcomes Ensure the accuracy and quality of pharmacometric analyses and reports Engage with regulatory agencies and prepare regulatory submission documents related to pharmacometric analyses Stay abreast of the latest developments in pharmacometrics and incorporate new methodologies and technologies as appropriate Present findings and strategies to the project team meeting and cross-functional teams. Ability to work effectively in a team environment.
Posted 1 week ago
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