Nandhini Jambunathan

Phone: 612-***-****

Mailto: accogq@r.postjobfree.com

Professional Summary

> An associate with Thomson Reuters, India from 2008 till 2012, with

total of 4+ years of work experience in the HealthCare Industry.

> Primary area of expertise is in Managing Clinical Data along with

strong expertise and experience in Clinical Database Management suite

and Handling Drug Data Report.

> Experienced in handling 15+ member clinical trial team with my last

held position as a project lead in Thomson Reuters, Chennai, India.

> Have exceptionally good experience in communicating, coordinating and

status reporting to overseas clients. Have communicated with Prous

Institute for Bio Medical Research, Barcelona all through my

experience with Thomson Reuters, India.

> Proficient in relational databases, database design, and software

tools to support data analysis and reporting. Familiarity with

database audits, discrepancy review, query generation and resolution

> Expertise in data querying and analytics tools, processes and

methodology and well versed in quality management methods and

healthcare processes.

Technology Summary

EDC Systems DB / General Software Experimental Pharmacology

Tools

Oracle Clinical SQL Prous Integrity Tool

Open Clinica MS Office

Research Tools / Techniques

Electrophoresis Chromatographic techniques Microbiology tests

Centrifugation Molecular biology procedures

Clinical Biochemistry

assays

Education Summary

> Masters Degree in Advanced Bio Chemistry from the University of

Madras, India securing the highest rank and an University Gold

Medallist.

> Bachelors Degree in Bio Chemistry passing out in the Distinction

Category. Possess proven track record on Academics and curriculum

right from the beginning of my education.

Certifications / Trainings

> ICH/GCP Certification for Clinical Trial Sites from Quintiles Global

Learning & Development in 2013, USA

> Training on Microbiology, Biochemistry and Hematology at Voluntary

Health services, Chennai, India

> Training in Immunology and Molecular biology techniques at Department

of zoology, University of Madras, India.

> Training program in Electron microscopy and Cytogenetics at Adyar

Cancer Institute, India

Research / Seminars

1. Research on the effect of Cadmium chloride induced toxicity

The research dealt with quantifying the protein contents of major

organs and lymphoid organs of Rattus

norvegicus exposed to Cadmium chloride induced toxicity and the

hematological parameters were also studied

in detail.

2. Brain cancer - Analyzing the biochemical status of Glioma patients

The research dealt with a comparative analysis on the overall biochemical

status of the normal and glioma

patient brain tissues and serum samples. The difference in DNA, matrix

metalloproteases and protein contents

were also studied using gelatin zymography, SDS PAGE, agarose gel

electrophoresis, western blotting.

Project Experience Summary

I.THOMSON REUTERS - 2008 - 2012

THOMSON SCIENTIFIC WAS ONE OF THE FIVE OPERATING DIVISIONS OF THE THOMSON

CORPORATION. THE SCIENCE UNIT OF THOMSON REUTERS PROVIDES INFORMATION-BASED

SOLUTIONS FOR THE ACADEMIC, BUSINESS AND R&D COMMUNITIES AND HAS PHARMACY

AND HEALTHCARE CLIENTS WORLDWIDE.

Client / Project#1 : Prous - Pre Clinical Experimental Pharmacology

Role: Process Lead

Location: Chennai, India

Period: May 2008 - Jun 2009

Responsibilities:

> Scientific analysis of medical journals, pre-clinical presentations,

thesis reports and providing comprehensive information on the

preclinical data like toxicology studies, biochemical, physiological,

Pharmacological or pharmacokinetic studies.

> Analysis of the safety and efficacy of potential drugs and updating of

this data in the database, according to the provided guidelines.

> Creation of new drug records in database by using clinical data from

online resources as well as from current press releases.

> Skills in managing a team and in collating of reports on a weekly

basis

Client / Project#2 : Prous - Drug Reporting and Clinical Trials

Role: Project Lead

Location: Chennai, India

Period: Jun 2009 - May 2010

Responsibilities:

> Scientific analysis of medical journals, drug data reports, clinical

presentations, thesis reports and providing comprehensive information

on the preclinical data like toxicology studies, biochemical,

physiological, Pharmacological or pharmacokinetic studies.

> Analysis of the safety and efficacy of potential drugs and updating of

this data in the database, according to the provided guidelines.

> Preparing abstracts for drug data reports.

> Creation of new drug records in database by using clinical data from

online resources as well as from current press releases.

> Skills in managing a team and in collating of reports on a weekly

basis

Client / Project#3 : Prous - Clinical Database Management

Role: Project Lead

Location: Chennai, India

Period: May 2010 - May 2012

Responsibilities:

> Support clinical trials for CRO by providing meticulous data

management. Design and maintain databases, queries, reports, graphics

and data-analysis tools; perform data entry, check reviews, database

audits and coding; and define and validate study protocols.

> Interpret, synthesize and present technical information to CRO

management and pharmaceutical and biotechnology clients.

> Work closely with Oracle Clinical developers on the design, testing

and implementation of study databases.

> Oversee data-management lifecycle of large clinical trials, composing

and verifying reports and results.

> Develop clear clinical data sets enabling the standardized collection

and analysis of massive amounts of cross-boundary data content in a

timely manner and with a high level of accuracy.

> Track progress of clinical studies, ensuring projects meet timelines

and quality expectations.

> Quickly mastered industry best practices in CRO clinical-study

procedures and data management.

> Excelled in managing high-priority projects and resolving data

discrepancies, errors and omissions with thoroughness and expedience.

> Facilitated the rollout of new EDC system that streamlined data entry

and improved data-analysis functions. Contributed to design and

development of new GUIs, validation components and reporting tools.

> Served as a primary trainer to peers on new EDC system

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