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Medical Reviewer, Clinical Trials, Adverse Even

Medical Reviewer. JOB Description: Conduct review and assessment of serious spontaneous reports of adverse events and perform causality assessment of clinical trials and solicited...

Medical Reviewer

Client - Pharma CompanyDuration - 12 MonthsRate - OpenTHERE ARE 6 POSITIONS WITH THE HIRING MANAGER. TELECOMMUTE IS OKAYMedical Degree is required.- Critical skills: good medical...

Medical Reviewer, Clinical Trials, Adverse Event,

Conduct review and assessment of serious spontaneous reports of adverse events and perform causality assessment of clinical trials and solicited reportsDetermine regulatory...

Medical Reviewer/Safety Reviewer

Reference # : 09-16365 Title : Medical Reviewer/Safety Reviewer Location : Abbott Park, IL Experience Level : Start Date : Thu, Sep 3, 2009 Description Responsibilities include...

Pharmacovigilance Associate

PHARMACOVIGILANCE ASSOCIATECOMPANY INFO:MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device industries. We specialize in the nationwide recruitment of clinical trials personnel.Our client is committed to being a global leader in health care and to helping change millions of lives for the bet...

Clinical Data Manager

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philos...

Associate Director of Global Safety

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philos...

Senior Regulatory Affairs Associate

  JOB SUMMARY/PURPOSE: The Senior Regulatory Affairs Associate will, under minimal supervision, coordinate, compile, and submit applications to FDA, the EU and other regulatory bodies as required. Works with development teams and management to ensure rapid and timely approval of new devices and continued regulatory support of marketed devices including review of labeling and...

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