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 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.
Remote · Canada
The Senior Biostatistician will lead statistical and programming operations for clinical trials, ensuring high-quality deliverables and adherence to project timelines. They will provide statistical expertise for study design, analysis, and reporting, while collaborating with data management and clinical teams.
Remote · Canada
The Principal Biostatistician will provide technical and operational leadership for clinical trial programs, ensuring sound statistical methodologies in study design and reporting. They will also mentor junior staff, contribute to protocol development, and ensure all activities comply with regulatory requirements.
Remote · Canada
The Associate Director provides technical and operational leadership for clinical trial programs, managing project teams and ensuring sound statistical methodologies. They also mentor staff, interact with clients, and support regulatory submissions while ensuring high-quality deliverables.
Remote · Canada
Lead statistical programming projects and resolve day-to-day technical issues to ensure high-quality, on-time deliverables. Develop and validate SDTM and ADaM datasets while ensuring compliance with regulatory standards and company SOPs.
Remote · Canada
Lead complex statistical programming projects and provide technical guidance to the programming team. Ensure high-quality deliverables for regulatory submissions while maintaining compliance with SOPs and CDISC standards.
Remote · Canada
The Associate Director will oversee project planning, communication, and execution of clinical research services while managing Project Managers and Senior Project Managers. They are responsible for ensuring quality deliverables, managing budgets and timelines, and facilitating cross-functional team efforts across various clinical development programs.
Remote · Canada
The Director of Project Management will oversee the planning, communication, and execution of clinical research services while managing a team of project management staff. They are responsible for strategic alignment, portfolio performance tracking, and ensuring all projects meet quality, operational, and financial standards.
Remote · Canada
The Director of Clinical Data Management will establish and control clinical data operations to ensure valid, secure databases that meet regulatory requirements. They are also responsible for managing project portfolios, budgets, and leading a team to achieve corporate objectives.
Remote · Markham, Ontario, Canada
The Sales Enablement and RFI Manager develops, writes, and finalizes responses to client Requests for Information (RFIs) and capabilities presentations. They also coordinate between Business Development and functional leaders while maintaining the RFI content database.
Remote · Canada
The IT Support Specialist will resolve technical support tickets via ServiceNow and manage the configuration and deployment of hardware. They are also responsible for system patch management, user account administration, and maintaining office equipment.
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 · Markham, Ontario, Canada, United States
The Principal Data Manager acts as the primary contact for data management deliverables and oversees hands-on tasks including database design, UAT, and data validation. They are responsible for project-level resource planning, managing database modifications, and ensuring compliance with clinical trial standards and sponsor requirements.
Remote · Canada
The Senior Clinical Data Manager leads data management activities, including project planning, database design, and ensuring high-quality deliverables for clinical trials. They also manage client relationships, provide training to team members, and support regulatory audits and inspections.
Remote · Canada
The Clinical Data Manager will plan, manage, and perform data processing activities while leading assigned projects to ensure compliance with sponsor requirements. They are also responsible for designing case report forms, validating clinical data, and supervising data entry personnel.
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.
