Clinical Data Management Jobs
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Search Results - Clinical Data Management Jobs
Warman O'Brien-Toronto
Senior Clinical Data Manager | Global CRO | Full Time | Remote North AmericaOur client is a well-established mid-sized CRO based in the Toronto Area and known for providing top-notch clinical solutions to a range of small and mid-sized Biotech...
Everest Clinical Research.-Canada
in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Clinical Data Managers for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere...
Pharma Medica Research Inc.-Mississauga
and clinical reports to ensure consistency, quality, and compliance with regulatory requirements.
Work closely with Pharmacokinetic/Stat/Data management team to evaluate the study data and results, providing insights to support decision-making and study...
Warman O'Brien-Canada
Senior Clinical Data Manager | Global CRO | Full Time | Remote North AmericaOur client is a well-established mid-sized CRO based in the Toronto Area and known for providing top-notch clinical solutions to a range of small and mid-sized Biotech...
Syneos Health-Montréal
content and ensures the clinical project team (CRAs/CeMs) is aware of the contractual obligations and parameters.
• Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables...
Everest Clinical Research-Markham
of special interests, concomitant medications, disease history, and early study termination due to AEs. Follow up on issues identified during the review until they are resolved.
• Coordinate with study Project Managers and Clinical Data Managers to maintain...
appcast.io -
Syneos Health-Montréal
specifications for appropriate content, and for grammar, format, and consistency.
Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
Serves...
Pharma Medica Research Inc.-Mississauga
design to ensure consistency with the study protocol and requirements from a clinical/medical perspective.
• Review output generated by the Clinical Data Management team with regards to consistency and relevance from a clinical/medical perspective.
• Act...
Syneos Health-Montréal
content and ensures the clinical project team (CRAs/CeMs) is aware of the contractual obligations and parameters.
• Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables...
SickKids-London
/support for Research IT and other relevant departments on implementation of clinical research processes and technologies that follow regulatory requirements (e.g., implementation of a validated data management solution for IITs).
• Function as consultant...
appcast.io -
Syneos Health-Montréal
content and ensures the clinical project team (CRAs/CeMs) is aware of the contractual obligations and parameters.
• Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables...
Groom & Associés / Associates-Montréal
Technical Knowledge:
• Strong understanding of quality management standards (ISO 9001, ISO 9000).
• Expertise in clinical research regulations (GCP, ICH E6, ICH E14).
• Familiarity with GDPR, data privacy principles, ALCOA++, and 21 CFR Part 11...
Syneos Health-Montréal
progress by the use of approved systems and / or tracking tools.
• Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported...
Groom & Associés / Associates-Montréal
Technical Knowledge:
• Strong understanding of quality management standards (ISO 9001, ISO 9000).
• Expertise in clinical research regulations (GCP, ICH E6, ICH E14).
• Familiarity with GDPR, data privacy principles, ALCOA , and 21 CFR Part 11...
Groom & Associés / Associates-Montréal
standards (ISO 9001, ISO 9000).
• Expertise in clinical research regulations (GCP, ICH E6, ICH E14).
• Familiarity with GDPR, data privacy principles, ALCOA++, and 21 CFR Part 11.
• Risk management, medical device vigilance, and pharmacovigilance experience...
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