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Clinical data management Jobs in Scarborough, ON
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Clinical data management • scarborough on
Clinical Data Management Specialist
Everest Clinical ResearchMarkham, York Region, CAData / Project Management
OncousticsToronto, ON, CAData Management Implementation Specialist
DatacenturyToronto, ON, CAClinical Data Manager
Everest Clinical Research Services IncMarkham, Ontario, CANSenior Manager - Master Data Management
DeloitteToronto, Ontario, CanadaData Analyst, Investment Data Management
Connor, Clark & Lunn Financial Group (CC&L)Toronto, ON, CASenior Manager - Master Data Management
Deloitte CanadaToronto, ON, CATest Data Management (TDM) Consultant
Astra North Infoteck Inc.Toronto, Ontario, Canada- Promoted
Officer, Data Management
Campfire CircleToronto, ON, CanadaResearch & Data Management – Senior Data Analyst
Indigenous Lands & Resources TodayToronto, ON, CAManager Data Management and Analytics
Rubicon PathMarkham, York Region, CAData Hub Engineer - Asset Management
ScotiabankToronto, ON, CAClinical Data Manager
Everest Clinical Research Services Inc.Markham, York Region, CAData Management Technical Architect
PeopleToGoMarkham, ON, CanadaRemote Senior Data Management Lead - Global Clinical Trials
Warman O'BrienToronto, ON, CA- Promoted
Lead - Clinical Study Management
Smith+NephewToronto, CanadaData Management Consultant
Onico SolutionsRichmond Hill, York Region, CASenior Manager-Master Data Management
AccentureToronto, ON, CASenior Data Management Analyst (1A)
TD BankToronto, ON, CA- Quebec City, QC (from $ 137,612 to $ 147,146 year)
- Burlington, ON (from $ 137,898 to $ 147,146 year)
- Montreal, QC (from $ 134,569 to $ 140,782 year)
- St. John's, NL (from $ 72,088 to $ 140,747 year)
- Toronto, ON (from $ 98,857 to $ 140,022 year)
- Old toronto, ON (from $ 98,857 to $ 140,022 year)
- Vancouver, BC (from $ 82,167 to $ 130,000 year)
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Clinical Data Management Specialist
Everest Clinical ResearchMarkham, York Region, CA- Full-time
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 Data Management Specialist 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 :
- Perform data entry and processing activities for assigned projects. These tasks are performed in a timely and accurate manner and in compliance with trial Sponsors’ requirements.
- Assist the primary Data Manager in performing data management activities. These activities include, but are not limited to, writing Data Management Plans (DMP; including specifying database integrity checks), designing clinical trial Case Report Forms (CRFs), designing databases, monitoring data flow, and quality control processes.
- Write draft DMPs using standard DMP template.
- Assist in defining and monitoring clinical trial data flow and quality control processes in accordance with corporate standard operating procedures (SOPs), Good Working Practices, and divisional guidelines.
- Assist in designing and reviewing patient CRFs and database schema. Test data capture / entry screens and edit specifications.
- Assist in designing databases following database design standards and conventions that have been established by the company or the trial Sponsor.
- Accurately and efficiently validate electronically captured data. Write clear queries on missing data and data points failing pre-defined range checks and / or logical checks.
- Assist in performing data quality control procedures during the trial and additional database closure checks at the end of the study.
- Validate and distribute study monitoring reports to internal and external study team members.
- Assist in resolving data coding discrepancies resulting from the coding of medical events, procedures, and medications.
- Maintain and prepare for final archival of data management documentation relevant to the assigned clinical trials.
- and assist the corporate archivist in assembling and archiving such documentation.
- Assist data management quality assurance (QA) personnel in performing QA procedures on trial CRFs, database schema and databases for assigned studies. These QA procedures include, but are not limited to, the following : performing line-by-line checks on subject data listings against completed CRFs; comparing database schema against annotated CRFs; comparing final paper CRFs against CRF images that were captured during the trial.
Qualifications and Experience :
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.ecrscorp.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.
Seniority level
Seniority level
Entry level
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Employment type
Full-time
Job function
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Research, Analyst, and Information Technology
Industries
Research Services, Pharmaceutical Manufacturing, and Hospitals and Health Care
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