Rakesh Nagilla
@rakeshnagilla
I’m a DMPK scientist and leader helping teams translate hit-to-lead strategies into human dose-ready programs.
What I'm looking for
I’m a DMPK scientist and leader with 20+ years of experience in the discovery and development of small and bi-functional molecules, including protein degraders and antibody recruiting molecules. I focus on cardiovascular, immunology, rare disease, immuno-oncology, and oncology therapeutic areas.
In my current role as Senior Director, DMPK at SK life science labs (formerly Proteovant Therapeutics), I manage DMPK activities and serve as the DMPK program representative for protein degradation programs. I ensure alignment of hit to lead and lead optimization strategies, coordinate in vivo and in vitro DMPK and biology studies with CROs, and maintain DMPK budgets.
Previously, at GlaxoSmithKline, I held leadership roles including Director and Director, FPD DMPK, where I directed DMPK programs across multiple discovery efforts. I performed PK/PD analysis for compound progression, delivered human dose prediction to enable FTIH studies, and partnered closely with medicinal chemistry, biology, safety/toxicology, regulatory affairs, and clinical pharmacology in a team setting.
I also bring operational and governance leadership: I chair the Institutional Animal Care and Use Committee (IACUC), oversee performance management for BS/MS/PhD-level scientists, and strengthen efficiency through DMPK-wide initiatives. I’m energized by turning high-quality experimental design, data review, and modeling into clear, decision-ready recommendations.
Experience
Work history, roles, and key accomplishments
Senior Director, DMPK
SK Life Science Labs
Nov 2021 - Oct 2024 (2 years 11 months)
Managed DMPK activities and served as DMPK program representative for protein degradation programs. Designed and coordinated in vivo/in vitro DMPK and biology studies with CROs, supported hit-to-lead alignment, maintained DMPK budgets, and performed human dose predictions.
Led DMPK activities across multiple programs and acted as DMPK program representative for in vivo/in vitro translation. Coordinated CRO-supported DMPK and biology studies, performed PK/PD analysis during lead optimization, and conducted human dose prediction to enable FTIH studies.
Managed DMPK activities and ensured alignment of hit-to-lead and lead optimization strategies with DMPK programs. Performed PK/PD analysis and human dose prediction for enabling FTIH studies, chaired the IACUC, and supported scientific peer review.
Managed DMPK activities for multiple therapeutic areas and served as DMPK program representative. Coordinated in vivo/in vitro DMPK and biology studies with CROs, performed PK/PD and dose predictions for first-in-human studies, maintained EPE budgets, and chaired the IACUC.
Managed a DMPK team of 5 scientists and led scientific activities across multiple small-molecule programs. Directed PK/PD work to support compound progression and human dose prediction for first-in-human studies, chaired IACUC representation, and maintained DMPK EPE budgets within the performance unit.
Contributed to a core DMPK team delivering a clinical candidate into first-in-human studies and served as program/project representative. Designed, conducted, and interpreted preclinical in vitro/in vivo DMPK and bioanalytical studies, supported experimental design and model knowledge across programs, and represented the group on the IACUC.
Supervised a team of 7 in vivo DMPK scientists and co-led an in vitro/in vivo group of 14 scientists. Designed and led preclinical pharmacokinetic studies, approved key reports (including in vitro assays such as P450 inhibition and plasma protein binding), coordinated PK studies for animal toxicity dose selection, and performed due diligence for CROs.
Supervised a team of 6 scientists and co-led an in vitro/in vivo group of 11 to deliver preclinical pharmacokinetics support. Designed and executed preclinical PK studies, modeled and interpreted PK data, coordinated PK studies for animal toxicity dose selection, and authored regulatory document inputs for early development plans.
Education
Degrees, certifications, and relevant coursework
Auburn University
Doctor of Philosophy (PhD), Pharmacokinetics
Ph.D. in Pharmacokinetics at Auburn University. Dissertation: stereospecific pharmacokinetics of ketorolac in large animal species and evaluation of an implantable delivery system for long-term therapy.
Auburn University
Master of Science (MS), Pharmacology
M.S. in Pharmacology at Auburn University. Thesis: effect of once-weekly treatment with MDMA on schedule-controlled behavior in rats.
BITS Pilani
Bachelor of Pharmacy (Honours), Pharmacy
B.Pharmacy (Hons.) at BITS Pilani in Rajasthan, India. Degree details beyond the program name are not provided.
Availability
Location
Authorized to work in
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