Trang chủ
NM

Nandagopal Manickam

121
5
2

Giới Thiệu Thành Viên

Tiểu sử

I Nandagopal M, M.Pharmacy (Pharmacology) Currently, I am working as a Scientific Manager (QC) – GOSTAR db at Excelra. Recently worked as a Manager – Senior Subject Matter Expert - Pharmacology (QA/QC of Biology, Biomedical, Clinical & Toxicology data curation), doing QA/QC of Scientific research Biological curated data for Elsevier Chemistry Biology databases [Reaxys Medicinal Chemistry (RMC), Reaxys at STRAIVE (A&I team), Chennai from 06th Oct’ 2010 – 07th July’ 2022. I have 12.0 years of experience in Biological data curation (Abstracting & Indexing) field for various scientific Experimental Pharmacology/Toxicology/ADMET drug discovery research data’s from Journals/Patents for Elsevier research database's [Reaxys Medicinal Chemistry (RMC) and Reaxys (PD/PK/PHARM/PNU)] and experienced in Extraction, QC and QA of Phamapendium Project: DILI, Recommended dose and Dose clean-up projects - Clinical and Preclinical data’s (FDA-Elsevier collaborative project). Also, I had additional 1.3 years’ experience in other organisations (Madha dental college – Pharmacology Lecturer; Biocon - Internship trainee in Preclinical RnD; GVK BIO – Informatics trainee). I have good work experience and pharma knowledge in icuration/QA/QC of Clinical Pharmacology db (PharmaPendium): Experienced in systematic literature review and scientific research with use of controlled vocabularies and ontologies in clinical research Knowledge of drug development process, clinical study designs and basic statistical concepts used in clinical trials. Experienced in development of summary level Clinical Trial Outcomes Datasets for meta-analysis in Pharmapendium db. Medicinal Chemistry db (RMC): Bioactivity/Bioassays/Target/Diseases/Biomodels/PD/PK/ADME/DMPK/binding/Protein interaction/molecular biology/mechanistic and Toxicity data are curated in the form as biological material, Target, Assays, Measurement, Metabolism, Transport, Quantitative, Qualitative and Tested/Not published results. I obtained my postgraduate degree M.Pharm (Pharmacology) at C.L Baid Metha college of Pharmacy in 2009 from The Tn. Dr. MGR medical University, Chennai, India. I am much interested in Core research of Pharmacology/Toxicology/ADMET database curation, drug discovery and neuropharmacology research. My long-standing aim is to be actively involved with Drug discovery data curation - Preclinical and Clinical research and in an area that I find as a fascinating research environment. Recent Job Responsibilities ➢ Quality control, Quality assurance, Pharm data analysis of manually curated scientific Journals/Patents biological data’s (Pre-clinical & Clinical PK) for Elsevier’s - Reaxys Medicinal Chemistry and Reaxys databases. ➢ QA – Excerption error protocol and report writer of excerpted files (Journals/Patents) sent by Elsevier. ➢ QA – Excerption error analyst (Root cause analysis, Corrective & Preventive actions - Curation errors) ➢ QC and QA of DILI, Recommended dose and Dose clean-up project data’s (FDA-Elsevier collaborative Project) ➢ RMC database end product SQA/Taxonomy QA analyst (Pilot project: db end product QA analyst). ➢ QC - Complete reviewing of manually excerpted scientific data’s and providing feedback in writing. ➢ In-charge for maintaining productivity and ensuring the produced file quality within the team. ➢ Responsibility in the development of productive team, goal setting and monitoring the team output. ➢ Ensuring excerption quality in excerpted documents, TAT requirements, delivery and team Targets. ➢ Ensuring consistency in team productivity & quality every month. ➢ Training of fresher’s and mentoring the team w.r.t excerption guidelines and its update. ➢ Continuous learning sessions and educational feedbacks related to excerption doubts clarification. ➢ Technical issues handling related to productive tools with innovative ideas. ➢ Team line management & People management PharmaPendium Project (DILI, Recommended dose, Dose clean up) ➢ Extraction of DILI Project data’s (FDA-Elsevier collaborative project) from June’ 2020 ➢ Extraction of Recommended dose and dose clean up data’s ➢ QC and QA of DILI, Recommended dose and Dose clean-up project data’s Certifications/Training and Projects @ SPi ❖ Trained &Certified in Silver Medal Leadership Program in Jan 7, 2017 Project entitled “To increase overall team productivity by tracking employee productive working hours through automated software (Desk Time study)” by Aspire University of SPi Global. ❖ Trained in Lean Six Sigma – Green Belt (Quality - DMAIC Approach) in 2015 Proposed a project “To improve the Assay mask excerption quality of RMC deliverables” ❖ Participated and presented a new venture project for SPi in Infinity Awards Program in 2016 - 17 Project entitled “Pharmacovigilance (PV) Solutions – A New Market Segment for SPi”. ❖ Trained in Right First Time (RFT) approach and 5S system ❖Trained in Root Cause Analysis (RCA), Corrective and Preventive actions (CAPA) approach

Học vấn

  • Sri Ramachandra University
    Bằng cấp B.Pharmacy
    Ngành học Faculty of Pharmacy
    Ngày bắt đầu 01/2003
    Ngày kết thúc 01/2007

Kinh nghiệm

ST

Manager - Senior Subject Matter Expert - Pharmacology (QA/QC)

Straive •

01/2010 – 01/2022 •

Abstracting & Indexing (Curation) of Research Journals and Patents - Drug discovery db

BL

TRAINEE

Biocon Ltd •

01/2009 – 01/2010 •

Preclinical R&D

MD

Lecturer

Madha Dental College and Hospital •

01/2010 – 01/2010 •

Department of Pharmacology

CM

M.Pharmacy (Pharmacology)

C.L.Baid Metha college of Pharmacy (The Tamil Nadu Dr MGR Medical University) •

01/2007 – 01/2009 •

Department of Pharmacology

GB

Trainee - Clinical pharmacology db

GVK Biosciences Private Limited •

01/2009 – 01/2009 •

Bioinformatics