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- 25 May 2015, 13:35
#314
VISIT: http://www.novartis.com/careers/job-sea ... unction=RD
https://sjobs.brassring.com/tgwebhost/j ... id=2364781
JOB DESCRIPTION:
Job ID 166343BR
Posting Title Trainee Writer
Division Pharma
Business Unit Development
Country India
Work Location Hyderabad
Company/Legal Entity India Novartis Healthcare Private Limited
Functional Area Research & Development
Therapeutic/Disease Area Oncology
Job Type Full Time
Employment Type Temporary
Job Description <1.Write clinical study reports under supervision of more experienced writers
2.Write patient narratives autonomously.
3.Quality check patient narratives written by other writers
4.Write safety documents (e.g. RMP, DSUR) under supervision from more experienced medical writer.
5.Act as a member of clinical trial teams following protocol finalization
6.Participate in planning of analysis and data presentation to be used in study reports, initially in conjunction with mentoring medical writer.
EEO Statement The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
Minimum requirements Education Qualification:- M.Sc Life Sciences, M.Pharma
•Candidate should be 2014 pass out
•Should have a minimum of 60% score in both Graduation & Masters
https://sjobs.brassring.com/tgwebhost/j ... id=2364781
JOB DESCRIPTION:
Job ID 166343BR
Posting Title Trainee Writer
Division Pharma
Business Unit Development
Country India
Work Location Hyderabad
Company/Legal Entity India Novartis Healthcare Private Limited
Functional Area Research & Development
Therapeutic/Disease Area Oncology
Job Type Full Time
Employment Type Temporary
Job Description <1.Write clinical study reports under supervision of more experienced writers
2.Write patient narratives autonomously.
3.Quality check patient narratives written by other writers
4.Write safety documents (e.g. RMP, DSUR) under supervision from more experienced medical writer.
5.Act as a member of clinical trial teams following protocol finalization
6.Participate in planning of analysis and data presentation to be used in study reports, initially in conjunction with mentoring medical writer.
EEO Statement The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
Minimum requirements Education Qualification:- M.Sc Life Sciences, M.Pharma
•Candidate should be 2014 pass out
•Should have a minimum of 60% score in both Graduation & Masters
