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March 17th, 2017

GVP Pharmacovigilance Audits – Senior GVP Audit/Project Manager Needed

Our client needs a full-time Senior GVP Audit/Project Manager to handle their GVP Pharmacovigilance Audits. This person will plan and perform domestic and international GVP audits to assess the company’s compliance to local and international government regulations. They will also assess internal SOPs as they relate to GVP Quality Assurance and regulatory compliance. This position is located Read the rest of this entry »

February 2nd, 2016

Clinical Affairs Director – TX or Upper Midwest

Clinical Affairs Director will lead and manage the Clinical Affairs Department globally, reporting to Read the rest of this entry »

January 8th, 2016

VP Medical Affairs in San Diego

Education & Experience:

May 15th, 2013

Sr. Manager/Director of Medical Education – Orange County, CA

As part of Global Medical Affairs, the Sr. Manager/Director of Medical Education is responsible for the successful execution of company Medical Affairs programs, including:

• Plan, manage and execute company’s New Customer Training and certification program worldwide, implement Staff and Surgeon training modules, develop strategies for training global field team.
• Associated to training and monitoring activities, the candidate will support implementation and execution of company’s podium and evidence plan, including:
o Planning, design, and execution of Read the rest of this entry »

May 8th, 2013

Clinical/Regulatory Medical Writer, Los Angeles CA

This position is for a medical writer with clinical and regulatory writing experience (not preclinical) and  will be based at Headquarters in the Los Angeles area (not home-based). Write clinical study reports, data summary reports, publications and promotional materials.

 

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