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Listed below are the top 10 out of 113 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Irvine, CA
$3,000 Sign on Bonus offered for Phase II Clinical Research Associates! ICON is experiencing tremendous growth, and we're looking for experienced Clinical Research ...
Adecco Engineering & Technical - Orange County, CA US
Adecco Medical & Science, a leading provider of contract and permanent staffing in the Pharmaceutical, Life Science Technology, Medical Device, and Health Care ...
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Licensed CLS with a strong immunology biology background (ELISA, IFA, Flow Cytometry) This position is open as of 5/12/2012. Are you a fit? Click Here to Apply ...
Adecco Engineering & Technical - Los Angeles, CA US
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Job Description: TITLE: Technical Group and Systems Associate Director LOCATION: Lake Forest, CA KimberlyClark is leading the world in essentials for a better ...
Adecco Medical & Science, a leading provider of contract and permanent staffing in the Pharmaceutical, Life Science Technology, Medical Device, and Health Care ...
Adecco Medical & Science, a leading provider of contract and permanent staffing in the Pharmaceutical, Life Science Technology, Medical Device, and Health Care ...
Description Perform SAS programming to implement Statistical Analyses Plans and SAS programming plans Create a statistical study report including all summary ...
RESEARCH/CLINICAL RESEARCH COORDINATOR II: Sought by CedarsSinai Medical Center in Los Angeles, CA. Bachelor's plus 4 yrs exp. Send resume to: Hao Nguyen, ...
For your reference, we have included the original job posting below.
Director, Clinical Scientist - Retina
Job Number:
42698456
Company Name:
Allergan
Job Location:
Irvine, CA US
Job Category:
Science & Biotech
Director, Clinical Scientist - Retina
The Clinical Scientist is the internal scientific expert in the disease area under study including scientific aspects of the competitive landscape. The Clinical Scientist is accountable for ensuring the medical/scientific validity and integrity of the clinical development program and study protocols. S/he plays a key role in supporting clinical study planning and execution throughout Development starting with the creation of the Clinical Development Plan (CDP) and clinical study protocol synopsi...