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Tushar

Tushar A. Patil is seeking a position with a reputed organization to develop his skills and contribute to the organization and nation. He has over 10 years of experience as a Clinical Research Associate with Macleods Clinical Research Center in Mumbai. His responsibilities include obtaining informed consent, preparing clinical study reports, administering drugs to subjects, and ensuring studies are progressed according to good clinical practice standards. He has successfully completed USFDA, ANVISA and WHO audits. Tushar holds an M.Pharm from Annamalai University and B.Pharm from R.C.Patel College of Pharmacy, both with distinction.

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121 views3 pages

Tushar

Tushar A. Patil is seeking a position with a reputed organization to develop his skills and contribute to the organization and nation. He has over 10 years of experience as a Clinical Research Associate with Macleods Clinical Research Center in Mumbai. His responsibilities include obtaining informed consent, preparing clinical study reports, administering drugs to subjects, and ensuring studies are progressed according to good clinical practice standards. He has successfully completed USFDA, ANVISA and WHO audits. Tushar holds an M.Pharm from Annamalai University and B.Pharm from R.C.Patel College of Pharmacy, both with distinction.

Uploaded by

api-3698598
Copyright
© Attribution Non-Commercial (BY-NC)
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Tushar A.

Patil
[email protected]
TUSHAR A. PATIL

PERSONAL PROFILE

MAILING ADDRESS: DATE OF BIRTH : 17 TH


APR 1984
H.N.-72, MMRDA COMPLEX CITIZENSHIP :
INDIAN
DURGA NAGAR, LINK RD GENDER :
MALE
(E),
JOGESHWARI MARITAL STATUS : SINGLE
MUMBAI-93, LANGUAGES KNOWN :
ENGLISH,HINDI,MARATHI.
INDIA.
Mob-09322152074
[email protected]

OBJECTIVE

To become a member of the team of experts of the reputed organization. This will provide
me an opportunity to develop my skills, education for continued self growth and enhancement of the
organization, in turn the nation.

PROFESSIONAL WORK EXPERIENCE

Presently working as a CRA with USFDA Approved Macleods Clinical Research


Center, Andheri, Mumbai, Since Sept.2007, till date.

JOB RESPONSIBILITIES
o To obtain inform consent from subjects.
o To prepare Clinical Study Reports as per ICH- E-3 and Review.
o To prepare IEC Summary Reports.
o Preparation of study Protocol
o Review of study Protocol
o Administering drug products to subjects during clinical study.
o Adverse Event Monitoring.
o Verifying and checking all raw data before Internal QA Audit.
o Writing and Revising SOPs as per need and maintain awareness of all current SOPs.
o Monitor Bioequivalence studies as per GCP and GLP.
o Ensure smooth progress of the Clinical Study.
o Archiving of Documents.

ACHIEVEMENTS

Faced Successfully USFDA Audit.


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Tushar A. Patil
[email protected]
Faced Successfully ANVISA Audit.
Faced successfully WHO Audit.

ACADEMIC PROFILE

M. Pharm. : Annamalai University, Dept of Pharmacy, Tamilnadu with Distinction


B. Pharm. : R.C.Patel College of Pharmacy, Shirpur, Dhule, Maharashtra, with Distinction
H. S. C. : New English and Junior College, Sakri, Maharashtra, with Distinction
S.S.C. : K.S.C.B.Vidyalaya, Dhadne with distinction.

INDUSTRIAL WORK EXPERIENCE

1. INDUSTRIAL PLANT TRAINING: IPCA LABS LTD, SILVAASA, (1 MONTH)

2. Project work on Bioequivalence study of fixed dose combination of


Lamivudine 150 mg and Stavudine 40 mg Tablet in Healthy Adult,
Male, Human Subjects under Fed condition carried out at Macleods Clinical
Research Center, Andheri, Mumbai.
.
REFERENCES

1. Mr. Amit Nakhe,


Sr. CRA,
Clinical Section,
Macleods Clinical Research Center.

2. Mr. Balwant Salunke,


Executive,
Clinical Section,
Macleods Clinical Research Center.

DECLARATION

The Information furnished above is true to the best of my knowledge and I


will take the complete responsibility in case of any circumstances.

Date :
Place: Mumbai. TUSHAR A. PATIL

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Tushar A. Patil
[email protected]

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