CDM

Responsibilities for this position include: clinical data management - actively working with clinical trials sites to ensure complete and accurate data collection and clinical data analysis.

* Generate clinical safety and efficacy data summaries for analysis by VP of Clinical Research and Director Clinical Research and for inclusion in regulatory packages, publications, corporate presentations, and diligence packages
* Research discrepancies in data and work with team members to resolve issues.
* Manage the review process for clinical research documents and new publications.
* Submit data for publication.
* Oversee development of CRFs, clinical and safety databases, and shell Tables, Figures and Listings, database freeze and database lock. Participate in data review meeting.
* Develop templates to assist in the data collection process
* Perform data entry, generate as well as manage tables and listings for assigned clinical studies ensuring security and quality of excel data entry tools.
* Audit technical data and information.
* Maintain appropriate databases and filing systems to ensure proper archiving.

Requirements
* BS in scientific discipline or pharmacy, RN or BSN degree or equivalent experience
* Oncology background or experience is preferredTo find out more about Real Staffing please visit www.realstaffing.com