Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post : Expert Scientific Writer
Job Description
To write, support and manage projects to prepare all high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, Manuscripts (complex) for publication/ presentation or for submission to regulatory authorities and/or clinical teams.
To write, support and manage projects to prepare all high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, Manuscripts (complex) for publication/ presentation or for submission to regulatory authorities and/or clinical teams.
Major Accountabilities
1. Prepares literature review, abstracts, posters, and slide sets, Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc.
2. Performs quality control (QC) checking / proof reading of the above mentioned documents to meet customer expectations.
3. Manages multiple projects across multiple brands at any given time.
4. Obtains feedback from customers; defines and implements customer management tactics.
5. Supports people and performance management.
6. Supports process improvement initiatives.
7. Complies with and support group’s project management tool, standards, policies and initiatives.
8. Follows Novartis specifications for documentation, specifically Novstyle, templates etc. 9. Follows and track clinical trial milestones for assigned projects.
10. Maintains records for all assigned projects including archiving.
11. Maintains audit, SOP and training compliance.
12. Trains new joiners, fellow colleagues as and when required.
13. Performs additional tasks as assigned.
1. Prepares literature review, abstracts, posters, and slide sets, Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc.
2. Performs quality control (QC) checking / proof reading of the above mentioned documents to meet customer expectations.
3. Manages multiple projects across multiple brands at any given time.
4. Obtains feedback from customers; defines and implements customer management tactics.
5. Supports people and performance management.
6. Supports process improvement initiatives.
7. Complies with and support group’s project management tool, standards, policies and initiatives.
8. Follows Novartis specifications for documentation, specifically Novstyle, templates etc. 9. Follows and track clinical trial milestones for assigned projects.
10. Maintains records for all assigned projects including archiving.
11. Maintains audit, SOP and training compliance.
12. Trains new joiners, fellow colleagues as and when required.
13. Performs additional tasks as assigned.
Candidate Profile
Minimum science degree or equivalent, B.Sc./equivalent with 10 years Clinical Research (CR) experience, M.Sc./M.Pharm +8 years of clinical research (CR) Excellent written and oral English Minimum: Minimum science degree or equivalent, B.Sc./equivalent with 10 years Clinical Research (CR) experience, M.Sc./M.Pharm +8 years of clinical research (CR) experience Desired – Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent) Ph.D + 6 year of CR experience, MBBS/equivalent + 6 year of CR
Minimum science degree or equivalent, B.Sc./equivalent with 10 years Clinical Research (CR) experience, M.Sc./M.Pharm +8 years of clinical research (CR) Excellent written and oral English Minimum: Minimum science degree or equivalent, B.Sc./equivalent with 10 years Clinical Research (CR) experience, M.Sc./M.Pharm +8 years of clinical research (CR) experience Desired – Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent) Ph.D + 6 year of CR experience, MBBS/equivalent + 6 year of CR
Additional Information
Experience : 5+ years
Qualification : B.Sc, M.Sc, M.Pharm
Location : Hyderabad, AP
Industry Type : Pharma
Functional Area : Research & Development
End Date : 25th February, 2019
Experience : 5+ years
Qualification : B.Sc, M.Sc, M.Pharm
Location : Hyderabad, AP
Industry Type : Pharma
Functional Area : Research & Development
End Date : 25th February, 2019
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