Dr. Arvindkumar Ghule Email & Phone Number

Pune

• Good understanding and experience of planning, designing and executing in-vivo / in vitro pharmacological experiments in multiple therapeutic areas like cardiovascular diseases, Inflmmation, pain, diabetes, diabetic complications and obesity. • Good knowledge of drug development and clinical research processes.• Immunopharmacological evaluation of NCE, immunogenicity studies, • invivo monitoring of immune responses during infection, inflammation. • pharmacological based analysis of immune targets, • Industry-academic collaboration and scientific writing

Pune

Team lead: Clinical data management and Biostatistical analysis teamAnalysis of clinical data by using SQL server and by using statistical software’s like R, Graph Pad Prism V, SPSS version 16, Instat, SAS jump.To write, edit, reconcile and manage high quality medical and scientific communications including manuscripts, literature review, abstracts, slide sets for publication/presentation or for submission to regulatory authorities and/or clinical teams.Follow and track clinical trial milestones for assigned projects.Prepare ADHOC report for regulatory authorities and/or clinical teamsPrepares manuscripts, literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles, protocols etc.Performs quality control (QC) checking / proof reading of literature review, abstracts, posters, and slide sets to meet customer expectations.

Pune Area, India

• Good understanding and experience of planning, designing and executing in-vivo/in vitro pharmacological experiments in multiple therapeutic areas like cardiovascular diseases, Inflmmation, pain, diabetes, diabetic complications and obesity. • Good knowledge of drug development and clinical research processes.CLINICAL RESEARCH SKILLS• Collation, acquisition, compilation and systematic documentation of relevant research details from Research Databases: Pubmed, Clinical Trials.gov, DARE, Embase, BIOSIS, CDSR, and CCRCT • Designing of Research protocols & Standard operating procedures for clinical studies. • Biostatistical analysis softwares used: Analysis of clinical data by using statistical software‟s like Graph Pad Prism V, SPSS version 16, Instat, SAS jump. • Published 28+ research papers in various peer reviewed international journals.• Presented research articles in various national and international conferences.Area of Interest: Medical / Scientific Writing Clinical / Preclinical Pharmacology

Mumbai Area, India

Development of the pharmacological screening models for preclinical evaluation of synthetic lead molecules for cardiovascular, diabetic complication, inflammation and immunoprotection. Data management: Preparation of research protocols and standard operating procedures (SOP) for animal studies. Biostatistical analysis softwares used: Analysis of clinical data by using statistical software‟s like Graph Pad Prism V, SPSS version 16, Instat, SAS jump.

Pune Maharashtra, India

Development of the pharmacological screening models for preclinical evaluation for various diseases such as cardiovascular diseases, Diabetes and its complication. Data management: Preparation of research protocols and standard operating procedures (SOP) for animal studies. PK-PD Study: pharmacokinetic and tissue distribution studies of various isolated biomolecules.

Doctor Of Philosophy (Phd), Pharmacology And Toxicology

M. Pharm, Pharmacology And Toxicology, First Class With Distinction

Graduate Aptitude Test In Engineering (Gate), Pharmaceutical Sciences