Sridivya

Sridivya

$10/hr
I am a assistant professor
Reply rate:
-
Availability:
Part-time (20 hrs/wk)
Age:
35 years old
Location:
Karimnagar, Telangana , India
Experience:
1 year
 RESUME VASALAMARRI SRIDIVYA email-H.NO:1-4-129 voice:- BRAHMIN STREET KARIMNAGAR OBJECTIVE: Looking for a challenging position in healthcare domain in an organization that would give an opportunity to enhance my technical skills and scope to learn offers professional growth and justify my education EDUCATIONAL QUALIFICATION: M.PHARMACY: David Memorial College of Pharmacy affiliated to Osmainia University Year:- (65%) B.PHARMACY: Vaageshwari Institute of Pharmaceutical Sciences affiliated to JNTU University Year:- (61%) INTERMEDIATE: Alphores Junior College Karimnagar Year:- (72%) SSC: Vindhya Valley High School Karimnagar Year: 2006 (78%) PERSONNEL STRENGTH: Self confidence and Eagerness to learn Research and Analysis skills SPECIALIZED SKILLS AND KNOWLEDGE: Basic competence Of Pharmacology with CVS/CNS/Respiratory/Endocrine System Drugs Therapeutic Terminology Familiar with Pharmacokinetic/Pharmacodynamic Parameters Good Knowledge Of Regulatory Affairs , ICH, EU ,Guidelines Ability to Work In Multidisciplinary Fields EXPERTNESS OF CLINICAL RESEARCH, PHARMACOVIGILANCE: Gained fair knowledge on clinical trials drug development process, IND/NDA/ANDA, USFDA, CDSCO, Responsibilities. Case intake :Responsible for case intake and duplicate check and registration Maintain log of source documents and other communications Case processor: Responsible for data entry of individual case safety reports into safety database. Review and evaluate AE case information to determine required action based on following internal policies and procedures, full data including coding and case narrative Medical coder: Coding Adverse events (MedDRA & WHO-DD) Case Narrative: Responsible for writing medically relevant safety narrative of cases and checking the completeness and and accuracy of data entered EXPERTNESS OF CLINICAL DATA MANAGEMENT: Utilize current study documentation including protocol, case report, conducting data review & identify report protocol. Understanding CRF Completion Guidelines Performed Data management tasks Preparing the Data Management Plan Create CRF completion guidelines User Acceptance Test Discrepancy management – Manual Query generation, Reviewing answered queries and closing the answered queries SAE Reconciliation Understanding on Study start up, Discrepancy Management and Study close out ACADEMIC PROJECT: Formulation and Evaluation of Liquid Solid Compact of OLMESARTAN MEDOXOMIL. AREAS OF INTREST: Pharmacovigilance, Clinical Data Management, Clinical Research, Regulatory Affairs Computer Skills: Ms Office Tools : Ms Word , Ms Excel , Ms Power point Operating System Tools : Windows XP, Windows 7, Windows Vista Networking Tools : Networking Trouble Shooting Problems PERSONAL DETAILS: Name: V.SRIDIVYA MARITAL STATUS: SINGLE LANGUAGES: English Telugu DECLARATION: I hereby declare that all the information provided by me in this application is factual & correct to the best of my knowledge & belief. Date: 17/09/2017 Place: Karimnagar Signature: V.Sridivya
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