| Job Description | Job Responsibilities:
Advise on, draft, and conduct statistical analysis plans for Phase II, Phase III, and pre-clinical animal studies and conduct the analysis plans.
Write statistical text for study concept documents and protocols (study design, endpoints, sample size, methods for analysis).
Create templates for tables, listings and graphs.
Oversee external partners and vendors.
Review protocols, clinical report forms, clinical study reports, and other study documents.
Help respond to the FDA on their queries to NDA submission.
Job Requirements:
Minimum of BS degree; experience in clinical trials a plus.
Must be comfortable with writing SAS code and directing others on writing SAS code.
Operating Systems – PC/SAS, Word. |
| | Company | | Hemispherx Biopharma Inc | Job Code | | State or Province | | Pennsylvania | | |
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