Project Data Entry

Ankit Patel

**L Tigertail Circle, Derry, NH *****

Contact no: (603) - 289-7752 E-mail: **************@*****.***

OBJECTIVE

• Get a challenging job in the field of clinical trial.

SUMMARY

• More than three year experience in, Clinical trial and trial related procedures, cGMP

manufacturing and retail pharmacy.

• Familiar with FDA and Pharmacy regulatory agency requirements.

• Flexible, self-motivated, able to work under optimal supervision and as a team player.

• Knowledge of cGMP manufacturing, cGMP facility, HIPPA, GCP and ICH guidelines

including understanding of regulatory requirements.

• Excellent organization, planning and problem solving abilities. Excellent negotiation and

analytical skills.

• Established interpersonal and communication skills.

SKILLS

• Proficient in Microsoft office (Word, Excel, Visio, outlook, project) computer and expertise

in searching information through web.

EDUCATION QUALIFICATION

Pharmacist’s License Expected: Mar 2015

Master of Pharmacy (Clinical Pharmacy).

A.R College of Pharmacy, Vallabh Vidyanagar, India.

Date of Graduation: July 2010

Bachelor of Pharmacy

The Oxford College Of Pharmacy, Bangalore, India.

Date of Graduation: Oct 2006

PROFESSIONAL EXPERIENCE

CVS Pharmacy

Pharmacy Technician: August 2012 – Present

• Assist pharmacist with prescription data entry, dispensing, inventory, ordering and re-stocking of

various medicine.

• Assist patients with insurance issues and provide proper guidance for insurance claim.

• Maintain patient records and other pharmacy related documents required to be in comply with

regulatory agency.

Cliantha Research Limited, Vadodara, India

Research Associate (Project Coordinator) Sep 2010 – Jan 2012

• Correspondence with sponsor, IEC, internal department for trial related activities like

designing of protocol, trial update, investigational product related issues, subject's safety

related issues and other study related issues along with the Principal Investigator / Head-

Clinical operation.

• Conduct of clinical trial in compliance with Protocol, in-house SOPs, GCP and applicable

regulatory.

• Providing training to clinical staff for study related activities according to SOPs and

Protocol requirements.

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• Monitoring and reporting of trial related activities.

• Reviewing of clinical study report.

• Providing solution to problems and seeking guidance whenever necessary

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Ravi Pharmaceuticals, Khambhat, India

Assistant Production Chemist June 2007- Nov 2007

• Assist in cGMP manufacturing activities like tablet manufacturing and its supportive

operations.

• Understand various cGMP flows like personnel flow, equipment flow, product flow through

out facility.

• To observe and understand rotary tablet machine, fluidized bed dryer (granulation), coating

process and packaging process.

• Understand role of quality department including control of raw materials and finished final

products.

• Perform various quality tests for tablets e.g. dissolution test, disintegration test, hardness test

and document results in log book.

Publication

I have published a research article on “study of drug utilization pattern of glucocorticoid

drugs with special emphasis on their immediate side effects in a tertiary teaching care

hospital” in Indian Journal of Pharmacy Practice (VOL3, ISSUE 4, Oct-Dec, 2010).

PROJECT AND TRAINING

(1) Post graduate training:-

Hospital: Shree Krishna hospital

Role: To recruit patients for clinical trial study, those were taking glucocorticoid drugs

for treatment. CRF were reviewed, required data were collected and analyzed.

Project title: To study the drug utilization pattern of glucocorticoid drugs with special

emphasis on their immediate side effects in a tertiary teaching care hospital.

Duration: September 2009 to May 2010.

(2) Under graduate training:-

Company: Vital formulation.

Role: To understand the cGMP flow, manufacturing facility, various processes like

cleaning, sterilization, manufacturing, packaging and labeling of Tablet, Soft and

Hard Gelatin Capsules, and Parenteral practically.

Project: Manufacturing, Sterilization, Mixing, Labeling and Packaging of Tablets, Soft

and Hard Gelatin Capsules and Parenteral.

Duration: Feb 2007 to March 2007.

WORK SHOP & SYMPOSIUM

(1) Participated in the “One day national level clinical carnival 2009” organized by

Darmsinh Desai University, at Nadiad (Gujarat).

(2) Participated in the one day symposium on “Opportunity in Clinical Research” held on

22nd October, 2008 organized by Baroda college of Pharmacy.

(3) Name of workshop: Drug design and discovery.

Description: Workshop was mainly on the Drug Design and

Discovery. Mainly to understand how drug is design. For desired

effect specific bond angle is required if it changes it can cause

side effect and toxic effect.

Company: INDGEN TECHNOLOGY PRIVATE LIMITED.

Duration: FEBRUARY 2006.

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