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| Team Lead-Medical writer, Associate Director
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| Write/QC ClinicalRegulatory submission document like Clinical Study Reports (Phase I and II),Patient Narratives integrated safety summary reports, integrated clinical study reports, Investigator’s Brochures (IBs), Investigational New Drug Applications (INDs), periodic safety updates, annual reports, occasional manuscripts for peer-reviewed journals, and other items for the medical community.
Knowledge of Regulatory procedures and Drug Safety regulations.
PhD, Experienced.
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| Resume reference: | baiaTJLB | |
| Date last updated: | May 6, 2008 | |
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| Education: | Post-graduate degree - PhD (Life sciences) | |
| Experience: | 5-9 years | |
| Employment situation: | In permanent employment | |
| Salary expectations: | best in par with industry | |
| Availability: | From November 2, 2008 | |
| Type of employment: | Full Time, Part Time | |
| Location: | Abroad - Mumbai, India | |
| Looking to work in: | BC/Vancouver, ON/Ottawa, ON/Toronto/GTA, QC/Montréal, QC/Québec | |
| Age: | 30 | |
| Gender: | Male | |
| Marital status: | Single | |
| Own transport: | Yes | |
| Driver's license: | Yes | |
| Citizenship: | Indian | |
| Right to work | No, I need sponsorship | |
| English level: | Advanced | |
| French level: | Zero | |
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