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/
Remote · Canada
The Clinical Trial Assistant will support clinical trial operations by managing essential documentation, maintaining TMF and CTMS systems, and coordinating with study sites and vendors. They will also assist in regulatory submissions, site monitoring compliance, and the preparation of clinical trial reports.
Remote · Canada
Support medical writing and safety monitoring teams through QC review of regulatory documents and data verification of statistical outputs. Manage document e-publishing, archiving, and provide secretarial support for DMC/DSMB meetings.
Remote · Canada
Direct the operational delivery of clinical trial safety services and lead the strategic expansion of post-marketing safety infrastructure from the US to a global scale. Manage regulatory submissions, aggregate reporting, and the financial performance of the safety business unit.
Remote · Canada
Lead the standardization of clinical trial data libraries by designing interactive BI dashboards and defining consistent metrics across business units. Support the full development lifecycle of CTT CDD applications through requirement documentation, testing, and client demonstrations.
Remote · Canada
Act as the primary lead and contact for clients regarding IWRS/IRT and eDiary solutions, ensuring high-quality data monitoring and issue resolution. Responsibilities include performing drug management analysis, executing UAT, and mentoring junior monitors to ensure compliance with SOPs.
Remote · Canada
The role serves as the primary contact for IWRS/IRT and eDiary users, providing technical support and issue resolution. Responsibilities include monitoring data accuracy, executing application testing, and maintaining requirements documentation.
Remote · Canada
The role serves as the primary contact for IWRS/IRT and eDiary users, providing overnight technical support and issue resolution. Responsibilities include monitoring data accuracy, executing application testing, and maintaining system documentation.
Remote · Canada
The role involves serving as the DMC Secretary, managing administrative tasks for committees, and supporting project management for clinical safety. Additionally, the associate performs quality control on regulatory documents and assists with safety event case processing.