AYESHA HABEEB

To carry out Experimental and Clinical Pharmacological Research in various therapeutic areas in strict compliance with Good Clinical Practice(GCP), Good Laboratory Practice(GLP) guidelines. To solicit a position in research and development department of a renown industry and to associate myself with a chance to update and contribute my knowledge. To collect, monitor and assess Adverse Drug Reactions(ADR) from Clinical Dept. in the Hospital. To design and assist in designing of Research Protocols in the area of Safety,Efficacy and Pharmacoeconomic drug studies. To prepare and review the manuscripts those are to be published in various National and International Medical and Pharmacy Journals. To coordinate with Institutional Ethics Committee and its members in Drug Regulatory, Safety Reporting and Protocol Proposal Acceptance aspects To be associated with progressive Organization as a Health Care Professional, This provides career development opportunities and contributes in its progress through my knowledge and skills and desire to make an effective contribution towards the growth of medical and health related content.