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 the operationalization of clinical trials by managing documentation, maintaining Trial Master Files, and coordinating with investigational sites and vendors. They will also assist with regulatory submissions, site feasibility, and the tracking of trial metrics to ensure compliance with ICH-GCP guidelines.
Remote · Canada
Develop and execute safety data review plans for clinical trials, focusing on AEs, SAEs, and laboratory data. Perform medical coding using MedDRA and WHODrug dictionaries while coordinating with data managers to ensure high-quality data collection.
Remote · Canada
The Senior Clinical Database Designer will develop and maintain clinical database designs, including eCRFs and EDC systems, to ensure efficient and accurate data collection. They will also oversee user acceptance testing, manage project timelines, and provide technical support to clinical trial teams.
Remote · Canada
The Senior Medical Writer authors regulatory documents such as clinical study protocols, reports, and briefing packages while ensuring compliance with sponsor styles and regulatory standards. They also lead writing projects, act as the primary client contact, and perform peer reviews to ensure high-quality deliverables.
Remote · Canada
The Medical Writer will prepare and QC clinical documents such as study protocols, CSRs, and scientific publications while ensuring adherence to project timelines. They will also perform literature searches, manage document e-publishing, and potentially serve as a DMC administrator.
Remote · Markham, Ontario, Canada, United States
The Manager will provide technical and operational leadership for clinical trial programs while managing client relationships and project deliverables. They are also responsible for mentoring staff, overseeing budget planning, and contributing to business development activities.
Remote · Canada
Design and maintain clinical databases for new studies using various electronic data capture (EDC) systems. Collaborate with data management teams to ensure data integrity, perform unit testing, and support regulatory compliance through quality audits.
Remote · Canada
The role involves standardizing clinical trial data reporting, developing interactive dashboards, and ensuring data accuracy across various business units. Additionally, the monitor will support clinical trial technology startup activities, perform user acceptance testing, and provide analytical support for product development initiatives.
Remote · Canada
The Clinical Data Management Specialist performs data entry, processing, and quality control activities for clinical trials in compliance with sponsor requirements. They assist in designing databases, writing data management plans, and validating electronically captured data to ensure high-quality study deliverables.
Remote · Canada
Serve as the Data Monitoring Committee (DMC) Secretary by managing committee recruitment, meeting coordination, and documentation. Support project management activities to ensure clinical trials are executed within timelines, budgets, and regulatory requirements.
Remote · Canada
The developer is responsible for the full-stack design, development, and maintenance of custom Java web applications within a clinical research environment. They will collaborate with cross-functional teams to gather requirements, perform system testing, and ensure the security and performance of web-based solutions.
Remote · Canada
Conduct PK/PD data analysis using non-compartmental analysis and support modeling and simulation tasks. Contribute to clinical trial protocol development, statistical analysis plans, and the authoring of regulatory documents and study reports.
Remote · Canada
The Senior Clinical Trial IWRS Monitor acts as the primary client contact for IWRS/IRT systems, managing study drug inventory, data quality, and issue resolution. They also lead system testing, provide training, and mentor junior staff to ensure deliverables meet quality and compliance standards.
Remote · Canada
The monitor acts as the primary contact for IWRS/IRT helpdesk support, managing client requests and resolving technical issues. They are also responsible for monitoring system data, executing application testing, and maintaining documentation for clinical trial systems.
Remote · Canada
The monitor acts as the primary contact for IWRS/IRT helpdesk support and ensures data accuracy within clinical trial applications. They are also responsible for executing system testing, maintaining documentation, and coordinating with study teams and sponsors.
Remote · Canada
Provide strategic clinical pharmacology and pharmacometric expertise to support drug development programs and regulatory submissions. Lead advanced PK/PD modeling and simulation activities while providing scientific mentorship to the team.
Remote · Canada
Lead clinical operations delivery for assigned studies across start-up, conduct, and closeout, ensuring quality, regulatory compliance, timelines, and budget commitments. Provide team leadership and oversight of site activation, monitoring, study documentation, vendor and site coordination, and resolution of risks and quality issues.
Remote · Canada
The manager will lead clinical data and safety monitoring operations, specifically focusing on the administration and project management of DMC/DSMB committees. They are responsible for mentoring team members, ensuring regulatory compliance, and driving departmental goals while maintaining strong client relationships.
Remote · Canada
The Manager will lead the medical and scientific writing functional area by planning, performing, and delivering high-quality regulatory documents while mentoring project team members. They are also responsible for recruiting and developing staff, managing client relationships, and contributing to business development and departmental process improvements.
Remote · Canada
Develop and validate SDTM and ADaM datasets and statistical output reports in accordance with clinical trial protocols and regulatory standards. Support clinical data acquisition and cleaning processes by performing data integrity checks and collaborating with data management teams.
