Job Description
Data extraction, cleaning, transformation and reporting using SAS and Excel . Use SAS procedures like proc summary, proc tabulate, proc means, proc univariate, proc ANOVA and excel pivot for marketing campaign.
Desired Candidate Profile
Applied knowledge on Logistic, Linear regression, segmentation. Communicating business results with clients and peers.
Experience : 1 - 3 Years
Location : Hyderabad / Secunderabad
Company Name : Client of Emilestones India
Executive Name: Nanda
Email id : nilotpala@emilestones.net
Telephone : 08041714296
18 February 2010
10 February 2010
Drug Safety Associate
Role Responsibility
You will be responsible for monitoring and tracking Serious Adverse Events, serious and non serious drug adverse reactions and other medically related project information. You will ensure that all ICON, Sponsor and Regulatory timelines are met for the processing ad recording of safety information.
Additional Responsibilities:
• Document and process serious adverse event reports within ICON, regulatory authorities and sponsor regulations and timeframes
• Provide input for and review relevant safety tracking systems fro accuracy and quality
• Perform safety review of clinical data (case report forms) and patient labs
• Assist medical monitor in documentation and processing routine exception and re-screen approvals
• Liaise with investigational sites and reporters on safety related issues
• Serve as medical resource to investigational sites and ICON personnel on safety related issues
• Perform safety related training for extra-department ICON staff
Experience and Qualification
With a science degree, pharmacy or nursing background you will have a minimum of 6 months to 1 years experience in a drug safety environment. You will possess excellent verbal and written communication skills and must be fluent in English. This will be combined with a good knowledge of medical terminology.
In addition you will also require:
•Good basic computer skills in MS office applications and data base use
•Produce high quality work and be detail orientated
•Be able to prioritise your work to meet required deadline
•Be willing to travel up to 10%.
Company Name : Icon Clinical Research India Private Limited
Experience : 1 - 3 Years
Executive Name: Neil
Email Address : Nilamadhab.Mahapatra@iconplc.com
Telephone : 04443902958
Department : Medical Safety
Location : Chennai
You will be responsible for monitoring and tracking Serious Adverse Events, serious and non serious drug adverse reactions and other medically related project information. You will ensure that all ICON, Sponsor and Regulatory timelines are met for the processing ad recording of safety information.
Additional Responsibilities:
• Document and process serious adverse event reports within ICON, regulatory authorities and sponsor regulations and timeframes
• Provide input for and review relevant safety tracking systems fro accuracy and quality
• Perform safety review of clinical data (case report forms) and patient labs
• Assist medical monitor in documentation and processing routine exception and re-screen approvals
• Liaise with investigational sites and reporters on safety related issues
• Serve as medical resource to investigational sites and ICON personnel on safety related issues
• Perform safety related training for extra-department ICON staff
Experience and Qualification
With a science degree, pharmacy or nursing background you will have a minimum of 6 months to 1 years experience in a drug safety environment. You will possess excellent verbal and written communication skills and must be fluent in English. This will be combined with a good knowledge of medical terminology.
In addition you will also require:
•Good basic computer skills in MS office applications and data base use
•Produce high quality work and be detail orientated
•Be able to prioritise your work to meet required deadline
•Be willing to travel up to 10%.
Company Name : Icon Clinical Research India Private Limited
Experience : 1 - 3 Years
Executive Name: Neil
Email Address : Nilamadhab.Mahapatra@iconplc.com
Telephone : 04443902958
Department : Medical Safety
Location : Chennai
01 February 2010
Clinical Analyst
Job Description
To do a research analysis on the clinical data.To usae the tools of analysis for the data analysis.
Desired Candidate Profile
A science graduate with good subject knowledge and with good exposure in clinical process.
Experience : 0 - 2 Years
Location : Chennai
Compensation: Rupees 1,75,000 - 2,75,000
Company Name: Pepo Technologies
Executive Name: Poornima
Address :
Pepo Technologies
7th main road,
Annanagar,chennai-40
CHENNAI,Tamilnadu,India 600040
Email Address:pepotechnologies@yahoo.com
Telephone: 44-91-9710905599
To do a research analysis on the clinical data.To usae the tools of analysis for the data analysis.
Desired Candidate Profile
A science graduate with good subject knowledge and with good exposure in clinical process.
Experience : 0 - 2 Years
Location : Chennai
Compensation: Rupees 1,75,000 - 2,75,000
Company Name: Pepo Technologies
Executive Name: Poornima
Address :
Pepo Technologies
7th main road,
Annanagar,chennai-40
CHENNAI,Tamilnadu,India 600040
Email Address:pepotechnologies@yahoo.com
Telephone: 44-91-9710905599
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