Description
Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.
Work Experience
COMPANY | POSITION HELD | DATES WORKED |
---|---|---|
(Confidential) | (Confidential) | 1/2005 - Present |
AstraZeneca | (Confidential) | 11/2003 - 4/2004 |
Education
SCHOOL | MAJOR | YEAR | DEGREE |
---|---|---|---|
Osmania medical College, Osmania University, Hyderabad, India | Medical course curriculum | 1977 | Bachelor Degree |
Accomplishments
Highlights:
Extensive experience with all the modalities of the clinical research, monitoring duties, Drug safety and Project management. Have written multiple abstracts and 7 articles in the respected national medical journals. Experience of doing a family practice for 9 years in India. Currently an active licensure to practice medicine in India. Would like to keep working in the clinical research or drug safety and acquire more exposure and thereby get more experienced.Companies I like:
Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.
Job Skills
Keywords
Responsibilities
Was given the total charge of 6 projects. The responsibilities included carrying out all the duties including all the regulatory submissions, all the day to day clinical work, assisting in the recruitment of the patients and advising them before and after the surgery, doing all the monitoring functions, CRF form completions, data cleaning, keeping a regular contact with the Investigator, Sponsor, IRB, helping the Investigator panel in preparation of various powerpoint presentations to be presented on National or International platforms, acquisition of grants or funding for the unfunded projects, supervising a score of personnel reporting directly,assign them duties, supervise and write a report on their performance. The work also included maintaining a regular databases for the projects, filing an SAE, arranging for site payments, maintainence of updated documents, protocol writing, ICF preparations, amendments to the protocol.