Clinical research associate Resume
|Desired Industry: Biotech
|Desired Job Location: vancouver/ seattle area, Washington
||Date Posted: 3/20/2009
|Type of Position: Full-Time Permanent
|Desired Wage: 40,000
||U.S. Work Authorization: Yes
|Job Level: Experienced with over 2 years experience
||Willing to Travel: Yes, More Than 75%
|Highest Degree Attained: MD
||Willing to Relocate: Yes
Seeking an opportunity to pursue a challenging career as a clinical research professional that provides an opportunity for application of the skills developed through knowledge, experience and to achieve growth for self and organization.
Ambitious and driven professional with expert knowledge of medical terminology, GCP, FDA, etc regulations.Over 4 years clinical trial monitoring experiences in multiple research area. Ability to multi-task with strong organization skills.Experience with molecular techniques, and ability to attention to details.Strong interpersonal skills. A-self-starter, can work efficiently on own initiative or can integrate easily into team environment.
Clinical Research Associate
Gleneagles Clinical Research Centre ,Beijing, China 2004-2005
Phase II clinical study of ENDOSTAR TM as treatment of lung cancer
Created check lists for initiation visit, interim and close up visit¡@
Ensured protocol compliance, ICH-GCP and other regulatory complicance at trial sites
Performed monitoring activities, which includes source documents verification of clinical data, manage investigational products and other trial related supplies. Ensured the timely reporting of study information, which includes safety reporting to relevant study team member and regulatory authorities.
Clinical Research Coordinator (Doctor) 1999-2003
Assisted Reproductive Technology Research Center
Tianjin central OB/GYN hospital, Tianjin, China
Credited with conducting successful, complex clinical trial for comparing two IVF treatments.
Resolved data discrepancies, managed database, ensured complete and accurate data reporting.
Involved in the study development and start-up process including reviewing protocols, designing, preparing Confidentially and Ethics document
Developed study documents, and project-specific CRA training.
Scheduled patient visits , took sample, maintained patient log, and patient care
Performed blood samples taken, ICSI , IVF ,ELISA, and PCR in the lab
Certificate for completion of John Molson School leadership workshop 2008
Volunteer Assistant 2006-2007
Jewish General Hospital, Montreal, Quebec
Socialized with each patient on the assigned units , listened to concerns , and complains
Checked in with charge nurse and forward appropriate issues to the nurse manager
Provided non-medical assistance with patient transportation
Bachelor of Science, Molecular and cell biology 2008
Concordia University, Montreal, Quebec
Tianjin Medical University, Tianjin, China
Clinical trial monitor
GCP, IRB protocol
patients screening and follow up
Knowledgeable of medical terminology Trial data management
Formulating source documents
Documented the Adverse Event
DNA/RNA ,RT/PCR ,protein extraction, electroporation and immunoassay
Perform cell culture , IVF, ICSI
strong team player
Excellent interpersonal and communication skills
Human Genome Project, Cancer Research, Traveling, Reading Scientific Journals
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