Clinical Research Manager

Negotiable

Full-time
Unlimited experience
Refresh at 8 months ago
15 Views
1 Apply
Shanghai
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Job responsibilities
1. Responsible for or participate in the design and writing of Phase I-IV clinical trial protocols, provide medical supervision and training in the trials, analyze and interpret test data after the trial is completed and write reports 2. Responsible for the preparation and writing of clinical relevant data required for registration and national major special applications
Job requirements
Clinical medicine related major
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Simcere Pharmaceutical Group
Medical institutions

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