Pharma Medical Clinical Research

CURRICULUM VITTAE

VESACHIYA DILEEPKUMAR BABUBHAI

*/*, ***********,

Nr. Jantanagar,

Amraiwadi road,

Ahmedabad – 380026.

Contact no. : +919*********(M)

E-mail : acdr79@r.postjobfree.com

OBJECTIVE

To associate with an organization that provides me an opportunity to show my techno

proficient skills, to improve my knowledge with the latest trends and to be a part of the team

that works dynamically towards the growth of the organization and my career.

PERSONAL DETAILS

Name VESACHIYA DILEEPKUMAR BABUBHAI

Address 1/8, Ashishnagar, Nr. Jantanagar,

Amraiwadi road, Ahmedabad – 380026.

Phone (M) +919*********

E-mail acdr79@r.postjobfree.com

January,4th, 1990

Date of Birth

Nationality Indian

Gender Male

Marital Status Unmarried

Languages Known English, Hindi and Gujarati

Hobbies Travelling, Reading, Music, Net surfing, Playing Chess and Carom.

EDUCATIONAL QUALIFICATION

Passing

Course/ Degree College/University Years Percentage

M.PHARM Gujarat 2013 6.68 C.P.I.

Technological University

Post-Graduation Focus Educare Pvt. Ltd., 2012 Completed

Ahmedabad

Diploma In Clinical

Research

FINAL B.PHARM 2010-11 62.38 %

T.Y B.PHARM 2009-10 64.38 %

Shree B.M Shah College Of

Pharmaceutical Education And

S.Y B.PHARM 2008-09 65.15 %

Research, Modasa

F.Y B.PHARM 2007-08 68.38 %

H.S.C. G.H.S.E.B., Gandhinagar 2007 74.00 %

S.S.C. G.S.E.B., Gandhinagar 2005 77.00 %

EXTRACURRICULUM

0 GPAT 2010 Qualified Certificate.

0 ICH-GCP Certificate.

0 NSS Volunteer under Youth for Rural Reconstruction Campaign Certificate.

0 Environment & Disaster Management Examination Certificate.

CORE COMPETENCE

0 Excellent grasping capability and understanding the concepts clearly.

0 Ability to work effectively while working as a team member as well as individually.

0 Problem solving skills.

0 Time punctual.

WORK EXPERIENCE

0• Completed training in GVK Biosciences Private Limited (Clinical Research

Organisation) as Contractual Research Assistant (Trainee).

Job Profile:

ICH-GCP, BA-BE studies, Protocol handling, Report generation, CRF, e-CRF prepation,

SOP Training, Data review, Site Initiation, Subject Recruitment, Reporting of Subjects,

ICF Presentation, Obtaining Inform Consent from Volunteers for participation in a study,

Check in Supervision, Meal Supervision, Dosing, Dosing Supervision, Phlebotomy

Supervision, Check-out Supervision, Investigators Meeting, Compilation of Raw Data,

Receiving, Handling, Dispensing and Storage of Investigational Products, Management of

Pharmacy, Compilation of Documents, Clinical studies Other Activities Delegated by PI..

AREA OF INTEREST

0• Clinical Research Associate, Clinical Research Co-ordinator, Clinical Data

Management, Clinical Analyst, Pharmacovigilance, BA-BE Studies, Clinical

Regulatory Affairs, SAS Programmer, Medical Clinical Co-ordinator, Medical Writer,

Technology Transfer, Medical Analysis, Electronic Medical Records, Medical Coding.

DECLARATION

I hereby declare that the information furnished above is true to the best of my knowledge.

Dileep B. Vesachiya

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