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Clinical Research Professional Experience

Location:
Pune, Maharashtra, India
Salary:
Negotiable
Posted:
January 13, 2018

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W wasFeral.S.Modi Address:

M.Pharm(Pharmacology) C1/702,Mantra Majestica

+917620567897 Kale padal road,Hadpsar

ac30sx@r.postjobfree.com Pune,411028

CAREER OBJECTIVE

To give the best services to the valuable oraganization by honesty,hard work and want to be an element to make organization successful.

Seeking a position to utilize my skills and abilities in organization that offers professional growth while being resourceful,innovative and flexible.

PROFESSIONAL EXPERIENCE

Worked as a Clinical Research Coordinator at Concept Clinical Research, Surat from 1 Jan 2016 to 30 Jun 2016.

ACADEMIC QUALIFICATIONS

Course

Year

College/University

Percentage

M.pharm (pharmacology)

2013

GujaratTechnologicalUniversity, Ahmedabad

7.17 CPI

GPAT

2011

M.S University of Baroda

Qualified

B.Pharm

2011

South Gujarat University, Surat

65%

H.S.C

2007

GSHEB, Gandhinagar

73%

S.S.C

2005

GSHEB, Gandhinagar

87%

JOB PROFILE

Complete Coordination of Phase-III/IV and BA-BE Clinical Trials as per ICH-GCP guidelines, Organization SOPS as well Protocol requirements on, which includes:

Screening, Randomization & Follow-up of subjects as per Protocol requirement.

Source documentation, Case Report Forms (electronic as well paper) entry, reporting of AE/SAE /Outcome events to Sponsor, CRO & EC as per protocol and regulatory guidelines.

Maintaining all documents related to study drug accountability including all shipping receipts/invoicing as part of the study file, Receipt of drug from sponsor for all studies, Maintaining Master Drug Accountability Log, Dispensing study drug to trial subjects & Instructing subjects regarding administration, proper method for handling & storage of study drug, monitoring & Complete record of temperature of study drug storage area.

Maintenance of trial specific Investigator Site File, Site-specific documents and all subject files.

Complete coordination between subject, Investigator and CRO from enrollment till end of trial.

Safety reports review and reporting to Ethics committee.

Ethics Committee Correspondence (including document submission)

Participation in Site Initiation Meeting, Routine Study Monitoring and Audits as well In-house Monitoring.

Dispatch of blood samples as per protocol requirement to Central laboratory.

Coordinating all activities and documentation from site identification to close-out

Developed a research naïve site to a good research site with precise pre-trial documentation in timely manner and clean documentation practice

BRIEF SUMMARY OF RELEVANT CLINICAL RESEARCH EXPERIENCE

Phase

Indication

Year

Completed/Ongoing

BE

RCC

2016

Ongoing

III

RA

2016

Ongoing

IV

Hormonal contraceptive device(IUD)

2016

Ongoing

IV

Valve replacement

2016

Ongoing

IV

Dyslipidemia

2016

Ongoing

CONFERENCES ATTENDED/PROJECTS

Poster presentation on “Autism disease” in state level UG Pharma presentation competition at Pharma excellence-09 held at C.K. Pithawala Institute of Pharmaceutical Science and Research,Surat-395007.

Poster presentation on “Advances in chemical and radiation carcinogenesis” held at Dharmaj Degree Pharmacy College, Dharmaj .

One day workshop on “Recent trends and techniques of cardiovascular research” held at, Uka Tarsadia University, Bardoli.

One day workshop on “Clinical Research- A Career Option” February 2012,held at, Uka Tarsadia University, Bardoli.

One day International Conference on “Nanopharmaceutical Therapeutics: From Laboratory to Clinical Practice” held at Shree Dhanvantary Pharmacy Colledge, Kim.

Review on Advanced in chemical and radiation carcinogenesis.

Research on Investigation of Antidepressant and anxiolytics effects of Curcuma longa extracts on chronic administration of some synthetic drugs in rats and mice.

TRAINING UNDERTAKEN

Undergone 3 months training at “Zota pharmaceuticals”,surat for the fulfilment of Bachelor in Pharmacy degree.

Online GCP training had taken on 22 Apr 2016 valid up to 22 Apr 2019.

RDC onsite training had taken on 13 May 2016

PROFESSIONAL PROFILE

I am “Registered Pharmacist “From 2012.

Highly organized and dedicated, with a positive attitude.

Ready to accept challenge from surrounding to achieve the best.

Believe in Perfection in Everything, Gives the Best of Myself.

Eager to learn regarding new Technologies.

Have excellent interpersonal communication skills.

Good explanation power.

PERSONAL PROFILE

Father’s Name Mr. Sureshchandra

Nationality Indian

Date of Birth 25th May 1990

Marital Status Married

Languages Known English, Hindi, Gujarati

Hobbies Teaching, Listening music

REFERENCES

1.Nimish Dudhatra

Director of Concept clinical service, Surat.

2. Vinod Vora

Clinical research coordinator at Concept clinical service, Surat

DECLARATION

I hereby declare that the above mentioned information given to the best of my knowledge & if you give an opportunity to work in our organization, I will put my best efforts.

Place: Pune

Date:

Feral. S. Modi



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