Must have Healthcare and Pharmaceutical experience
Project Description:
- Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions.
- Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead.
- Able to support multiple protocols independently and to contribute to integrated summaries of efficacy and safety.
- Demonstrates strong SAS programming skills; participates in protocol team and some project team interactions.
- Builds successful relationships and seamless interfaces at the protocol/project team level.
- Provides timely and effective communication to the programming and statistics leads.
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