Experience: 0 to 1 yrs. Posted on: 14 Feb
Walkin Interview from 17th February to 18th February from 10 AM
Experience : 0-1 year experience in Pharma/Clinical research.
Education: B. Pharm, M. Pharm etc
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.
Following up with sites regarding outstanding queries.
Follow up on reconciliation of discrepancies.
Follow departmental AE workflow procedures
Closure and deletion of cases
Perform any other drug safety related activities as assigned
Perform literature review activities when trained and assigned.
Basic competence with medical and therapeutic terminology.
Ability to work independently but guided by documented procedures, with appropriate support.
Able to work effectively as part of a team.
Understanding of patient safety regulatory obligations.
Should be familiar regulatory & pharmacovigilance guidelines.
Should be familiar with pharmacovigilance terminology.
Excellent attention to detail.
Ability to deliver within established timelines.
Fluency in English and excellent comprehension.
Computer literate.
Requires a proactive approach and excellent written/oral communication and interpersonal skills. Strong interpersonal skills required to interact with clients, management, and peers effectively. Effective cross- department communication. Ability to document and communicate problem/resolution and information/action plans.
Person should be familiar with MS Office Tools.
Safety database knowledge.
The ability to contribute to a team environment with a high degree of professionalism and skill. Demonstrate flexibility within a dynamic, fast-paced, cross-functional team. Demonstrated ability to complete multiple tasks concurrently and deliver results in a fast-paced environment. Ability to perform under stringent timelines.
VENUE:
1. #120P-122P, Belagola Industrial Area,
K.R.S. Road,, Metagalli,
Near GRS Fantasy Park,
MYSORE,
Karnataka - 570017,India
2. #120/A, Elephant Rock Road,
Jayanagar 3rd Block
BANGALORE,
Karnataka,India
CONTACT PERSON :
1. Affan at Bangalore
2. Sania at Mysore
Experience : 0-1 year experience in Pharma/Clinical research.
Education: B. Pharm, M. Pharm etc
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.
Following up with sites regarding outstanding queries.
Follow up on reconciliation of discrepancies.
Follow departmental AE workflow procedures
Closure and deletion of cases
Perform any other drug safety related activities as assigned
Perform literature review activities when trained and assigned.
Basic competence with medical and therapeutic terminology.
Ability to work independently but guided by documented procedures, with appropriate support.
Able to work effectively as part of a team.
Understanding of patient safety regulatory obligations.
Should be familiar regulatory & pharmacovigilance guidelines.
Should be familiar with pharmacovigilance terminology.
Excellent attention to detail.
Ability to deliver within established timelines.
Fluency in English and excellent comprehension.
Computer literate.
Requires a proactive approach and excellent written/oral communication and interpersonal skills. Strong interpersonal skills required to interact with clients, management, and peers effectively. Effective cross- department communication. Ability to document and communicate problem/resolution and information/action plans.
Person should be familiar with MS Office Tools.
Safety database knowledge.
The ability to contribute to a team environment with a high degree of professionalism and skill. Demonstrate flexibility within a dynamic, fast-paced, cross-functional team. Demonstrated ability to complete multiple tasks concurrently and deliver results in a fast-paced environment. Ability to perform under stringent timelines.
VENUE:
1. #120P-122P, Belagola Industrial Area,
K.R.S. Road,, Metagalli,
Near GRS Fantasy Park,
MYSORE,
Karnataka - 570017,India
2. #120/A, Elephant Rock Road,
Jayanagar 3rd Block
BANGALORE,
Karnataka,India
CONTACT PERSON :
1. Affan at Bangalore
2. Sania at Mysore
Interview Tips
Whether you are an experienced clinical research professional or applying for your first job, it is important to convey a competent and confident self in an interview. Here are some tips to help ensure success in an interview.
Always dress professionally for an interview
First impression is everything and how you present yourself to an interviewer is how they will perceive you would present yourself to a vendor, customer, government authority or member of the management team. Even if you know their environment is casual, always dress professional for an interview.
Always show enthusiasm during the interview
Showing enthusiasm and energy in an interview is very important. The ability for someone to get the job is just as important as their ability to do the job. Your enthusiasm, excitement and passion about the position and company will stick with the interviewer and it could be the difference between being chosen over another candidate who didn't express the same amount of enthusiasm.
- See more at: http://blog.cliniindia.com/p/interview-tips-whether-you-are.html#sthash.1Twtf8E5.dpuf
Whether you are an experienced clinical research professional or applying for your first job, it is important to convey a competent and confident self in an interview. Here are some tips to help ensure success in an interview.
Always dress professionally for an interview
First impression is everything and how you present yourself to an interviewer is how they will perceive you would present yourself to a vendor, customer, government authority or member of the management team. Even if you know their environment is casual, always dress professional for an interview.
Always show enthusiasm during the interview
Showing enthusiasm and energy in an interview is very important. The ability for someone to get the job is just as important as their ability to do the job. Your enthusiasm, excitement and passion about the position and company will stick with the interviewer and it could be the difference between being chosen over another candidate who didn't express the same amount of enthusiasm.
- See more at: http://blog.cliniindia.com/p/interview-tips-whether-you-are.html#sthash.1Twtf8E5.dpuf
Interview Tips
Whether you are an experienced clinical research professional or applying for your first job, it is important to convey a competent and confident self in an interview. Here are some tips to help ensure success in an interview.
Always dress professionally for an interview
First impression is everything and how you present yourself to an interviewer is how they will perceive you would present yourself to a vendor, customer, government authority or member of the management team. Even if you know their environment is casual, always dress professional for an interview.
Always show enthusiasm during the interview
Showing enthusiasm and energy in an interview is very important. The ability for someone to get the job is just as important as their ability to do the job. Your enthusiasm, excitement and passion about the position and company will stick with the interviewer and it could be the difference between being chosen over another candidate who didn't express the same amount of enthusiasm.
- See more at: http://blog.cliniindia.com/p/interview-tips-whether-you-are.html#sthash.1Twtf8E5.dpuf
Whether you are an experienced clinical research professional or applying for your first job, it is important to convey a competent and confident self in an interview. Here are some tips to help ensure success in an interview.
Always dress professionally for an interview
First impression is everything and how you present yourself to an interviewer is how they will perceive you would present yourself to a vendor, customer, government authority or member of the management team. Even if you know their environment is casual, always dress professional for an interview.
Always show enthusiasm during the interview
Showing enthusiasm and energy in an interview is very important. The ability for someone to get the job is just as important as their ability to do the job. Your enthusiasm, excitement and passion about the position and company will stick with the interviewer and it could be the difference between being chosen over another candidate who didn't express the same amount of enthusiasm.
- See more at: http://blog.cliniindia.com/p/interview-tips-whether-you-are.html#sthash.1Twtf8E5.dpuf
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