POSITION: |
Supervisor, Medical Writing |
LOCATION: |
Biovail Contract Research |
REPORTING TO: |
Manager,Medical Writing and Regulatory Affairs |
POSITION DESCRIPTION: |
- Preparing all Study Reports from projects conducted within Biovail Contract Research (BCR)
- Supervise and direct Medical Writers and external contractors as needed
- Scheduling, coordinating, writing and/or reviewing/ editing-protocols and final reports for Phase I studies, IVIVC studies and bioequivalence/bioavailability studies
- Interact with clients of BCR and with clinical and laboratory operations of the BCR
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QUALIFICATIONS & EXPERIENCE: |
- Bachelor or Masters degree in a health or biological science discipline.
- A minimum of three years experience in medical or scientific writing in a pharmaceutical context.
- Must possess excellent writing and computer skills complemented by strong project management and leadership abilities.
- Must have sound knowledge of GCP and ICH guidelines and full comfort with scientific and medical terminology.
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| CONTACT: |
Submit your resume to: jobs@biovail.com
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