Description
To obtain a challenging position within the Pharmaceutical industry or medical devices industry that will allow me to use my experience to play a key role in Clinical Research studies and projects, and/or product development with medical devices.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| Eisai Inc | Project Manager | 2/2014 - 3/2015 |
| Sanofi-Aventis | Documentation Specialist / Scientist II | 1/2008 - 3/2012 |
| Aventis Pharmaceuticals | Documentation Specialist / Scientist I | 8/2004 - 12/2007 |
| Aventis Pharmaceuticals | Associate Scientist/ Manager of Archives | 3/2000 - 8/2004 |
Education
| SCHOOL | MAJOR | YEAR | DEGREE |
|---|---|---|---|
| Q-Tech Solutions Professional Development Center | Clinical Research Associate Training | 2013 | Certification Degree |
| DeVry University | Technical Management | 2005 | Bachelor Degree |
| Union County College | Medical Laboratory Technology | 1990 | Associate Degree |
Social Media
| TYPE | TITLE | URL | DESCRIPTION |
|---|---|---|---|
| Book | Diane Carney LinkedIn | media url | LinkedIn account |
Accomplishments
Highlights:
Job Skills
| Microsoft Office |  |
| Documentum (First Doc) | |
| GRESDA | |
| S@T-TOX | |
| Provantis, Artemis, Path Data, Xybion | |
| GLP, GMP, GCP, ICH | |
| CFR Title 21 Part 11 | |
| SDLC | |
| Blood Borne Pathogens, OSHA | |
| QAAD, and CAPA | |
Keywords
