A global healthcare leader, 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: Medical Writer II
Job Description:
• To support Development by authoring, coordinating and managing the production of Clinical Study Reports
•Writing, editing and co-coordinating preparation of Clinical Study Reports (CSR)
•Drive the CSR process and coordinate a medical and scientific team within a matrix
•Participate in review of analysis plan and advise on required tables
•Develop and maintain effective working relationships among document contributors on multifunctional platforms
•Ensure reviewers and other contributors are identified and can perform tasks according to the agreed process
•Ensure CSR process is completed according to SOP within the time specified by the SOP or otherwise agreed with the team, which ever is shorter.
•CSR tracking and status reporting, including identifying milestone timelines
•Develop both the CSR process and product to match changing business needs
Candidate Profile:
•Higher education background (M.Sc., Ph.D., etc) including research experience and publications
•Highly literate and fluent in English
•Fluency in written and spoken English with strong ability to interpret and present data
•Two years experience of clinical or related research in an academic or industrial setting
•Objective and accurate interpretation of data and express findings in a clear and concise manner
•Ability and initiative to work independently and as part of a team
•Travel - Occasional- for trainings and meetings
Additional Information:
Job ID: 130625BR
Education: M.Sc, Ph.D
Industry Type: Pharma/Biotech/Clinical Research
End Date: 30th Nov, 2013
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