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JOB TITLE: Clinical Research Associate
LOCATION: Los Angeles, US-CA
JOB TYPE: Contract

HOURLY RATE: $64 - $68

DESCRIPTION:
SUMMARY OF WORK TO BE PERFORMED:
* Perform on-site, site evaluation and monitoring visits for clinical trials
according to the monitoring plan and policies and procedures
* Schedule and confirm study site visits and make travel plans, in accordance
with travel policy
* Review source documents and CRFs
* Collect, review and evaluate completed CRFs


* Follow up on Serious Adverse Event reports
* Attend training meetings on protocol, Standard Operating Procedures, Working
Practice Documents, and other monitoring and administrative-related topics
* Perform other such tasks as the manager may designate.

EXPERIENCE:
3-5 Years Experience
Pharmaceutical Experience

SKILLS:
Primary Skills: Phase 2-3 clinical trial monitoring, knowledge of computer
technology (i.e., Excel, Word, e-mail, utilizing a laptop)
Secondary Skills: Monitoring experience with opiods or pain trials; experience
with controlled substance trials
Basic computer technology skills (i.e.,Word, Excel, e-mail, etc.): Candidate
must have a home office setup, including the following: Phone and fax line
Personal office computer (ideally a laptop) High-speed connection to the
internet (i.e., cable modem, ISDN, etc.) Printer (ideally an HP)

EDUCATION:
Bachelors Degree

OTHER:
Secondary Work Location: Traveling to multiple states and possibly Canada
Hours Per Week: 50
Percentage of Travel Expected: 50%

MANDATORY SKILLS:
Clinical Research;Clinical Trials;Pharmaceuticals

MANDATORY EDUCATION: Bachelor

Please refer to Job#: 01240835-TE in all correspondence about this job.

ITECH CONSULTING PARTNERS, LLC
John Barry
Apply for this Job, please click on the link below.
http://www.topechelon.com/applyjob.asp?JobID=01240835NG

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