Uploading your resume is the best way to connect to our talent managers.
Including medical directors, drug safety, biostatisticians, clinical research associates, regulatory and quality professionals.
Finding experienced leaders with a history of bringing drugs or medical devices like yours to market.
When you need capable workers on a project basis or to fill in while a critical staff member is away, experts are available.
Through our Foundation, a unique model to on-board and properly train new hires in the life sciences industries
Senior-level auditors for pharmacovigilance, data management, quality systems, GMP, GCP and GLP audits
Ensure your team generates high-quality data and stays on track toward meeting your next regulatory milestone.
Sales Analyst for Pharmaceutical Company – 1yr Contract Our large pharma client in Irvine, CA is in need of a Sales Analyst on a temp to hire basis. We are one of the few agencies that pays 65% of health insurance costs. MINIMUM REQUIREMENTS: • Bachelor’s degree in Business, Computer Science, or Information Technology, Healthcare […]
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How Do Clinical Trial Sites Work? Clinical trial sites work to serve both patients and sponsors. They are critical to the advancement of medical science. Clinical trial sites are where drugs, medical devices and other therapies are tested on human beings. That data is then used by sponsors for FDA Approval of the product. This guide […]
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Resume Writing Ten-Day Challenge – $10 Your browser does not support the video tag. Improve your resume with this 10-day challenge on time and if you’re not satisfied we will refund your money. This challenge will teach you how to: write a better summary use the summary to guide your career uncover things that […]
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Regulatory Affairs Compliance Manager – Dietary Supplements in Orange County Client is seeking a Regulatory Affairs Compliance Manager to ensure regulatory compliance is implemented and followed at this high-volume contract manufacturer of dietary supplements. Client is in need of someone with manufacturing experience in FDA-regulated products such as pharmaceuticals, over the counter drugs, or dietary supplements. […]
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Associate Clinical Trial Manager – 6 month temp in Irvine CA Our client is in need of a Associate Clinical Trial Manager for one year temp to hire in order to assist in the operational execution of assigned clinical studies. Qualifications / Experience: • B.A/B.S. in science or health-related field • Two (2) years clinical […]
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Head of Quality for Dietary Supplements – Orange County Client is seeking a Head of Quality to ensure best practices are implemented and followed at this high-volume contract manufacturer. Requirements Director-level or higher position in Quality a high-volume manufacturing Experience managing large teams and indirect reports Manufacturing experience should include FDA-regulated products such as pharmaceuticals, […]
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Providing staffing, executive search, GxP auditing and recruiting for life sciences & bio-science companies.
100 N. Brand Blvd, Suite 306
Glendale, CA 91203
info@meirxrs.com
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