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Including medical directors, drug safety, biostatisticians, clinical research associates, regulatory and quality professionals.

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Finding experienced leaders with a history of bringing drugs or medical devices like yours to market.

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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

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Senior-level auditors for pharmacovigilance, data management, quality systems, GMP, GCP and GLP audits

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Ensure your team generates high-quality data and stays on track toward meeting your next regulatory milestone.

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MEIRxRS Blog and News


Associate Clinical Trial Manager - 6 month temp in Irvine CA

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

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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Resume Writing Ten-Day Challenge - Just $24

Resume Writing Ten-Day Challenge  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 you might […]

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FSPCA FSVP Training May 2018, Long Beach, CA

FSPCA FSVP Training May 2018, Long Beach, CA This course will provide participants with the knowledge to implement the requirements of the “Foreign Supplier Verificalinktion Programs (FSVP) for Importers of Food for Humans and Animals” regulation of the U.S. Food and Drug Administration (FDA). This regulation is one of a number of regulations and guidance […]

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Clinical Research Project Manager Needed RemoteWork

Clinical Research Project Manager Needed – Remote Work Clinical Research Project Manager needed by our client to manage clinical trials and to ensure on time regulatory submission. Requirements Bachelor’s-level degree required in science/health related field. Nine years of clinical research and/or clinical project management experience (roles such as CRA, CTA, Project manager, CRC etc..) at pharmaceutical […]

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IRB Regulatory Coordinator Temp Needed in West Los Angeles

IRB Regulatory Coordinator Temp Needed in West Los Angeles Growing Oncology Clinical Trial site needs a temporary IRB Regulatory Coordinator in the west side of Los Angeles. This is a temp to hire position. Responsibilities: Will provide support for clinical research protocols, informed consents, etc. Will assist with all aspects of clinical research regulatory to ensure compliance to […]

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