CURRICULUM VITAE

M.R. PRADEEP

acpcvf@r.postjobfree.com S/O Mr. P.Maharajan,

+91-978*******-**/10W, Suruli Street,

Chinnamanur-625 515,

Theni Dist,

Tamilnadu

OBJECTIVE:

To seek a challenging assignment and environment that encourages continuous learning and

provides exposure to new ideas for both personal and professional growth.

EDUCATIONAL QUALIFICATION:

Master in pharmacy,(August 2008 to May 2010)

SASTRA University,

Thanjavur-613401, Tamilnadu

Percentage: 67 %

Bachelor in Pharmacy, (September 2003 to August 2007)

JSS College of Pharmacy,

Ooty-643 001, Tamilnadu

Percentage: 67 %

WORKING EXPERIENCE:

• Worked as a Medical safety analyst in Accenture Services PVT LTD, Chennai,

(from Feb 2012 to Jan 2015).

• Worked as a Associate research analyst in Thomson reuters, Chennai, (from

Dec 2010 to Jan 2012).

• Worked as a Clinical Research Coordinator and Clinical Study Pharmacist

in Meenakshi Mission Hospital & Research Centre, Madurai, (from Sep.2007 to

Aug.2008), under Dr. Kirushna Kumar, MD (RT), Senior Consultant.

ROLES AND RESPONSIBILITIES:

Medical safety Analyst

• Encode verbatim terms using MedDRA for patient history, product indication, and

event term information.

• Enter labelling information for all client suspect products.

• Responsible for writing narrative summaries on reported adverse event cases.

• Overall review of literature article and attributing the adverse event with the suspect

drug and summarize the narrative relevant to the case.

• Responsible for completing the adverse event case; and sending the updated and related

documents.

• Perform daily responsibilities in accordance to all applicable Standard Operating

Procedures (SOPs), conventions and client policies.

• Plan, organize, and manage daily work to meet service level timelines and deliverables.

• Work with the Safety Review team lead to escalate issues or tasks outside the normal

scope of work.

Associate research analyst

• Updating clinical and strategic information.

• Investigation of drug developmental status.

• Consensus sales information and sales forecasting.

• Analysis of patent and trial reports.

Clinical Research Coordinator and Clinical Study Pharmacist

• Setting up the study centers, which includes ensuring each centre has the trial materials.

• Administered informed consent, document processes as per ICH and GCP guidelines,

obtain appropriate documentation, waivers.

• Serious Adverse Event reporting as per protocol requirements, DCGI guidelines to Sponsor

and regulatory authorities.

• Analysis of the clinical lab reports in conjunction with investigator and escalating the

medical queries to medical monitor if any.

• Coordinate scheduled visits, protocol based tests, laboratory evaluations.

• Responsible for query generation and query resolution arising during the database entry.

• Communicating deviations from the protocol, SOPs, GCP, and the applicable regulatory

requirements to the investigator and taking appropriate action designed to prevent

recurrence of the detected deviations.

EXPERTISE:

Typing skill - 30 to 40 Words / Min. with 90% accuracy.

Basics in computer

STRENGTH:

Team worker

Adaptable character

Disciplined

PERSONAL DETAILS:

: 4th June 1985

Date of Birth

Languages Known : English and Tamil

Marital Status : Single/male

DECLARATION:

I hereby declare that the above furnished details are correct to the best of my knowledge and

belief.

Place:

Date:

Yours faithfully

(M.R.PRADEEP)

Contact this candidate