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| Name of the Candidate | : | [Private] |
| Name of the Post Applied | : | Clinical Research Lecturer |
| Job related skills / software | : | To design and assist in designing of Research Protocols in the area of Safety, Efficacy, Pharmacoeconomic drug studies, To prepare and review manuscripts those are to be published in various National and International Medical Journals. |
| Category | : | Teaching Lecturer Faculty |
| Sub Category | : | Lecturer |
| Years of Experience | : | 4 years |
| State | : | Madhya Pradesh |
| Gender | : | Female |
| Salary Expected per Month(Rs) | : | 30,000 to 40,000 |
| Highest Qualification attained | : | P.G.D. / PGD : Post Graduate Diploma |
| Major / Specialization | : | Clinical Research & Management |
| Email Id | : | [Private] |
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| Are you looking for job now? | : | Yes |
| Can the recruiter contact you? | : | Yes |
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Resume Format / CV Sample Template / Example / Model : |
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CURRICULUM VITAE :
Dr. Mitali Porwal Augustya
W/O Major Dr. Priyank Augustya
Mail ID :- drmitali.porwal AT gmail.com/ mitaliporwal AT rediffmail.com
REGISTRATION NO :- A-2339
CAREER OBJECTIVE :-
Trained, detail oriented and thoughtfulprofessional prepared to excel in the field ofClinicalResearch / Pharmacovigilance / Pharma marketing and contribute to organizational objectives.
PROFESSIONAL QUALIFICATION :-
** X Board MP Board 79%
** XII Board MP Board 75%
** B.D.S. Jiwaji University 67%
** Post graduate diploma in Clinical Research and Management IICRM NAGPUR Grade A
** Master of Hospital Administration IICT Lucknow Grade A
EXPERIENCE :-
** 2.5 years of working experience as Senior Process Associate in Tata Consultancy Services (TCS), Mumbai in Pharmacovigilance Department.
** Currently working as lecturer at Clinical Research Institute .
CORE RESPONSIBILITIES :
** To carry out Experimental and Clinical Pharmacological Research in various therapeutic areas in strict compliance with GCP, GLP guidelines.
** To collect, monitor, assess and report Adverse Drug Reactions from Clinical Deptto National and International Pharmacovigilance Centre.
** To design and assist in designing of Research Protocols in the area of Safety, Efficacy, Pharmacoeconomic drug studies.
** To prepare and review manuscripts those are to be published in various National and International Medical Journals.
** To co ordinate with Institutional Ethics Committee and its members in Drug Regulatory, Safety Reporting and Protocol Proposal – Acceptance aspects.
** To train fellow and fresher Residents in various Research aspects.
** To present seminars, and participate in critical appraisal of various published scientific papers
** Handled all types of LEGAL and LIVE cases including logging of cases, triaging and complete data entry procedures in Pharmacovigilance.
** Also have good knowledge of Medical coding.
TECHNICAL SKILLS :
Proficiency in Windows, MS Office.
OTHER QUALITIES :
** Excellent verbal & written communication skills.
** Good computer knowledge.
** Good Interpersonal Skills.
LANGUAGE KNOWN :Hindi, English
EXPECTED SALARY :-Negotiable.
HOBBIES :-
Reading ,writing articles and poems, watching movies and cooking.
PERSONAL DETAILS :
Date of Birth : 20th Feb 1985
Marital Status : Married
DATE :
PLACE :
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