Clinical Trial IWRS Monitor I
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $45,000–$65,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- A Bachelors’ degree in health science, physical or biological fields with at least 3 years’ experience in clinical trial data processing and management.
Clinical Trial IWRS Monitor (Overnight)
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $45,000–$65,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- A Bachelors’ degree in health science, physical or biological fields with at least 3 years’ experience in clinical trial data processing and management.
Senior Clinical Trial Analytics Monitor I
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $100,000–$120,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Aptitude to learn and retain CTT CDD application rules and support procedures and broader related clinical trials processes to effectively troubleshoot and…
- IQVIAToronto, ON
- $116,300–$193,800 a year
- May act as a lead clinical manager alongside other clinical managers for the execution of large-scale international clinical trials.
- IQVIAToronto, ON
- $141,900–$263,500 a year
- Full-time +1
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Principal Biostatistician
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $150,000–$200,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or multiple clients.
Senior Biostatistician
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $110,000–$160,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Provide statistical expertise for design, analysis and reporting of clinical trials and research projects.
- Plan and conduct or contribute to the trial results…
- IQVIAMississauga, ON
- $124,400–$165,800 a year
- Full-time +1
- Knowledge of clinical trials - Knowledge of clinical trial conduct in addition to skill in applying applicable clinical research regulatory requirements i.e.
- CAMHToronto, ON M6J 1H4
- $100,475.26–$150,712.90 a year
- Full-time
- Dental care
- Paid vacation
- Extended health care
- Support Research Legal in the review of clinical trial agreements, as needed.
- The CTU supports CAMH researchers in the conduct of clinical trials through an…
- サイネオス・ヘルスToronto, ON
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work.
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- サイネオス・ヘルスToronto, ON
- $80,600–$175,700 a year
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
- Assess quality of the data.
- サイネオス・ヘルスToronto, ON
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work.
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- サイネオス・ヘルスToronto, ON
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work.
- サイネオス・ヘルスToronto, ON
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work.
- サイネオス・ヘルスToronto, ON
- $80,600–$145,000 a year
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work.
- サイネオス ・ヘルスToronto, ON
- Up to $210,900 a year
- Employee stock purchase plan
- Paid time off
- Vision care
- Dental care
- Paid sick leave
- Company car
- Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work.
Paid Clinical Trials jobs in Toronto, ON
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Job Post Details
Clinical Trial IWRS Monitor I - job post
Job details
Pay
- $45,000–$65,000 a year
Job type
- Permanent
Location
Benefits
Pulled from the full job description
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
Full job description
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. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.
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.
To drive continued success in this exciting clinical research field, we are seeking a committed, skilled, and customer-focused individual to join our winning team as a Clinical Trials IWRS Monitor for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.
Key Accountabilities:
- Act as primary contact with CTT Users for the Everest IWRS/IRT and eDiary team via the CTT Helpdesk telephone or IWRS helpdesk email accounts.
- Support client request and issue analysis, problem solving, and resolution, working closely with CTT Developers and internal Everest Data Management and Statistical & Programming teams.
- Monitor data generated within CTT applications to ensure accuracy and quality. This includes daily checks of automated data queries built in the CTT applications, as well as weekly manual checks of the data generated from the system.
- Coordinate and verify changes to the database and application using appropriate change control procedures and ensure comprehensive and accurate documentation is completed.
- Act as off-hours escalation point for junior IWRS Clinical Monitor resources or the outsourced call centre service to resolve high urgency client requests (based on agreed rotational schedule amongst IWRS Clinical Trials Monitor resources).
- Generate, maintain, and/or review CTT Requirements Specification documents.
- Execute CTT application test planning, test plan, and test script development and Stage I and II testing activities for CTT applications (newly developed applications or application change requests). These tasks are performed in a systematic and very detailed manner using the CTT Requirements Specification document as the base for testing CTT functionality.
- Generate, maintain, and/or review Quick Reference Guides for all CTT studies.
- Conduct CTT demonstrations to sponsors as well as training demonstrations to study team members.
- Support communications and coordination with Sponsors, Study Team Members, Depot personnel and internal Everest data management and statistical leads across the IWRS development lifecycle.
- Cooperate with and assist, when required, data management quality assurance (QA) personnel in performing QA procedures on CTT applications.
- Analyze CTT monitoring and support trends to identify new CTT core features that will improve efficiency, effectiveness, user satisfaction and market competitiveness to support CTT product development planning.
- Provide analytical, report generation, and project execution support to CTT and Everest management team members for internal CTT capability development initiatives.
Qualifications and Experience:
- A Bachelors’ degree in health science, physical or biological fields with at least 3 years’ experience in clinical trial data processing and management.
- Education or experience must demonstrate the ability to work independently, to have a clear, professional and energetic telephone voice, and detailed approach to data review and system development.
Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $45,000 - $65,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com (http://www.everestclinical.com)
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
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