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Experienced Data Coordinator Relocating to Dallas, Texas
I am looking for a company where I can add to my extensive list of Data Coordinator skills as well as share my skills with others. Working for a company which fosters the expansion of knowledge, is constantly growing and supports its employees is very important to me.
Clinical Data Management
About Me
Industry: |
Science & Biotech |
---|---|
Occupation: |
Clinical Data Management |
Highlights: |
At my current company, I am part of a team who won the Team Excellence Award for successfully locking 7 databases in 6 months. |
Education level: |
Bachelor |
Will Relocate: |
Yes |
Work Experiences
8/2007 - Present
(private)Individual Contributor
- ? Employs excellent project management skills while handling several studies at once. Using the below skills, has locked as many as seven studies in six months. ? Analyzes data for a plethora of clinical trials in the fields of Neurological Disease, Pediatric Eczema, Multiple Sclerosis, Infectious Disease, Pain Management, Lymphoma and Rosacea. ? Efficiently manages projects by maintaining and reconciling several clinical databases at once by generating queries, tracking Case Report Form pages, writing and reviewing edit checks and performing database updates; and performing Quality Control and Assurance Audits. ? Effectively reviews CRFs, CRF design, source documents, data listings, the electronic clinical database and external vendor transfers to ensure that all captured data follow the rules outlined by the protocol, Good Clinical Practices and Data Management Plan. ? Proficiently drafts Data Management Plans, Tracking and Data Entry Guidelines, Self- Evident Corrections and CRF Completion Guidelines based on study protocol and client needs. ? Expertly generates paper and electronic queries to appropriate internal or external personnel (i.e., investigational sites, vendors, Clinical Research Associates, client representatives) to resolve problematic data identified during every aspect of the data management process. ? Regularly corresponds with study site personnel and Study Sponsors to effectively identify and solve Data Management problems. ? Successfully follows studies from study start-up to study completion, including database freeze and lock procedures.
3/2006 - 8/2007