Everest Clinical Research

About

Everest Clinical Research ("Everest"​) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Operating primarily in North America, with headquarters located in Markham, Ontario (Greater Toronto Area), Canada, with additional offices in Bridgewater, New Jersey, USA, Shanghai, China, Taipei, Taiwan, and Sofia, Bulgaria, Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success

Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us…that's Everest!

Important Information for job candidates:
Please be aware of cyber-security due to some fraudulent job scams.
Everest will follow our standard and thorough recruitment process which will include video panel interviews: https://www.ecrscorp.com/recruitment-process/
Everest email communication will come from an ecrscorp.com email address.
Emails from other domains may not be from Everest.
Everest will never ask for credit card information or charge fees at any time during the recruitment process.
If something is portrayed as Everest but does not appear to be from Everest, please feel free to contact us at https://www.ecrscorp.com/contact/

Keywords

biostatistics, statistical programming, clinical data management, medical writing, dmc, dsmb administration, clinical operations, trial master file management, clinical project & site management, site monitoring, regulatory consultation, regulatory submission & lifecycle management, pharmacovigilance, drug safety, clinical trial services staff placement, interactive response technologies irt, iwrs, clinical epro & ediaries

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