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Drug Safety Associate Resume Sample, Experience : 2 years

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Name of the Candidate:[Private]
Name of the Post Applied:Drug Safety Associate
Job related skills / software:Responsible for data entry of individual case safety reports into the safety database, Review and evaluate AE case information to determine required action based on and following internal policies and procedures
Category:Medical
Sub Category:Drug Safety Physician
Years of Experience:2 years
State:Andhra Pradesh
Gender:Female
Salary Expected per Month(Rs):50,000 to 60,000
Highest Qualification attained:Diploma
Major / Specialization:Pharmacy
Email Id:[Private]
 
Are you looking for job now?:Yes
Can the recruiter contact you?:Yes
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Resume Format / CV Sample Template / Example / Model :

    

SAI SINDHU
Doctor of Pharmacy [Pharm D]
Mailid  :subhaprakashsindhu123 AT gmail.com

CAREER OBJECTIVE :
By acquiring knowledge , expertise and familiarity with the organizations culture that enables me to develop myself as a professional , I want to contribute my skills and expertise towards the growth of the organization.

WORK EXPERIENCE :
ICON PLC , Chennai.
Drug safety associate (May 2021 to present)

Essential duties and responsibilities  :
As case intake member  :-
** Responsible for case intake, duplicate check, and registration
** Maintain log of source documents and other communications

As Case Processor  :
** Responsible for data entry of individual case safety reports into the safety database.
** Review and evaluate AE case information to determine required action based on and following internal policies and procedures
** Process all incoming cases in order to meet timelines
** Full data entry including medical coding and safety narrative

As Medical coder  :
Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD)

As Narrative writer  :
Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.

As Literature review specialist  :
** Ensure effective and accurate collection, recording, review and reporting of literature searches conducted.
** Review of literature articles to identify case safety reports.
** Responsible for operational Pharmacovigilance activities for assigned developmental and/or marketed products.
** Assist in signal generation and safety analysis activities.
** Ensure quality of literature searches and reporting.
** Review of local/global literature reports to determine regional reportability.
** Create/maintain study summary documents.
** Assist with narrative writing for periodic/ad hoc submissions.
** Assist with ad hoc or routine safety monitoring activities.

Other responsibilities  :-
** Follow up for PMS , Sponsored clinical trial , RAVE and non sponsored clinical trial cases.
** Performed Follow up attempts by phone using cisco ip communication.
** Assigned cases for the team , worked on KPI metrics , throughput and also involved in management activities.

Computer Proficiency  :-
Data bases  :- Argus
Office tools  :- Microsoft word , excel , power point, Well versed with the internet.

ACADEMIC PROFILE :
** Doctor of pharmacy Sree vidyanikethan college of pharmacy , Tirupati JNTU Anantapur 2021 80%
** Intermediate Narayana Junior College, Nellore Board of secondary Education,A.P.


2014 91%
** SecondarySchool Vignan jyoti concept school, Varadaiahpalem Board of secondary Education,A.P. 2012 95%

INTERNSHIP EXPERIENCE :
** Clinical pharmacist intern in Sri venkateswara institutes of medical sciences – JNTU Ananthapur , Andhra Pradesh .
** Clinical pharmacist intern in Manipal Hospitals , Bangalore , Karnataka .

ACADEMIC PROJECTS :
A project entitled “ASSESMENT OF QUALITY OF LIFE IN BREAST CANCER PATIENTS UNDERGOING CHEMOTHERAPY IN A TERTIARY CARE HOSPITAL”.

CERTIFICATIONS :
** Completed an online course on “CLINICAL RESEARCH” from PHARMACON SOCIETY OF PHARMACY PRACTICE.
** Participated in workshop on pharmacovigilance and reporting of adverse drug reactions(SVIMS ,Tirupati). Certified in online course on NIDA Clinical Trials Network. ( feb 2nd , 2020)

PERSONALDETAILS  :
Dateof Birth  : 28-06-1997
Languages  : English – Articulate.Telugu – Native language

DECLARATION :
I,here by,declare that the information furnished above is trueand correctto best of my knowledge.

PLACE  :
DATE  :

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