Richard R Poelling

Senior Manager Regulatory Affairs @Dechra

Overland Park, KS, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Jul 2021 — Present

Senior Manager Regulatory Affairs @Dechra

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Overland Park, KS, US

EDUCATION

1994 — 1998

University of Missouri-Columbia

Bachelor of Science (B.S.), Biochemistry

2010 — 2012

Northeastern University

Master of Science (M.S.), Regulatory Affairs for Drugs, Biologics and Medical Devices

SKILLS

CmcU.s. Food and Drug Administration (Fda)Analytical ChemistryClinical TrialsDrug DevelopmentR&DQuality AssuranceClinical DevelopmentClinical SuppliesMolecular BiologyBiotechnologyResearch and Development (R&D)Cross-Functional Team LeadershipPharmaceuticsPharmaceutical IndustryFdaLife SciencesGlpRegulatory AffairsLifesciencesProject CoordinationGmp

ABOUT RICHARD R POELLING

Pharmaceutical Scientist with 20+ years of R&D and regulatory experience in drug development from preclinical through Phase 3 clinical studies in the pharmaceutical industry. Experienced in the management of clinical supplies for Phase 1 – 3 studies in the US and abroad, including regulatory compliance and adherence to program timelines. Maintains the necessary skill set to analyze and implement regulatory strategies to comply with diverse governmental sources such as OSHA, EPA, NRC and FDA. Generates and reviews documents from diverse sources and technical fields for quality assurance and regulatory compliance.

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Richard R Poelling — Senior Manager Regulatory Affairs at Dechra in Overland Park, KS, US | Unifers