The Data Manager will lead the development, implementation, and continuous improvement of research data management practices supporting the Clinical, Biospecimen, Imaging and Genetic (C-BIG ...
The Data Manager will lead the development, implementation, and continuous improvement of research data management practices supporting the Clinical, Biospecimen, Imaging and Genetic (C-BIG ...
Data Manager
Montreal, QC · On-site
The Data Manager will lead the development, implementation, and continuous improvement of research data management practices supporting the Clinical, Biospecimen, Imaging and Genetic (C-BIG ...
Data Manager
Montreal, QC · On-site
The Data Manager will lead the development, implementation, and continuous improvement of research data management practices supporting the Clinical, Biospecimen, Imaging and Genetic (C-BIG ...
Senior Director/Team Head--Oncology Late Stage Data Review
Kirkland, QC · On-site
CA$214K - CA$358K/yr
Effectively partners with other clinical and medical colleagues, clinical operations, data management, digital, and other functional lines for the successful implementation and execution of the ...
Senior Director/Team Head--Oncology Late Stage Data Review
Kirkland, QC · On-site
CA$214K - CA$358K/yr
Effectively partners with other clinical and medical colleagues, clinical operations, data management, digital, and other functional lines for the successful implementation and execution of the ...
Data Platform Architect
Montreal, QC · Hybrid
About the Role TailorCare is a value-based musculoskeletal (MSK) care platform combining clinical ... Proven track record designing production data platforms at scale, streaming and batch, with managed ...
Data Platform Architect
Montreal, QC · Hybrid
About the Role TailorCare is a value-based musculoskeletal (MSK) care platform combining clinical ... Proven track record designing production data platforms at scale, streaming and batch, with managed ...
Verifies required clinical data entered in the case report form (CRF) is accurate and complete. * Manages reporting of protocol deviations and appropriate follow-up. * Applies query resolution ...
Verifies required clinical data entered in the case report form (CRF) is accurate and complete. * Manages reporting of protocol deviations and appropriate follow-up. * Applies query resolution ...
Sr CRA - Canada (Quebec/Montreal)
Quebec, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
Sr CRA - Canada (Quebec/Montreal)
Quebec, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
What We're Looking For * 3+ years of relevant data engineering or data management within an ... clinical research for institutions that matter * Strong foundation: Series A, top-tier investors ...
What We're Looking For * 3+ years of relevant data engineering or data management within an ... clinical research for institutions that matter * Strong foundation: Series A, top-tier investors ...
What We're Looking For * 3+ years of relevant data engineering or data management within an ... clinical research for institutions that matter * Strong foundation: Series A, top-tier investors ...
Quick apply
What We're Looking For * 3+ years of relevant data engineering or data management within an ... clinical research for institutions that matter * Strong foundation: Series A, top-tier investors ...
Manage nursing protocols Collect data from standardized clinical data sheets and assess clinical situations Perform various administrative tasks on the computer Answering questions from parents and ...
Manage nursing protocols Collect data from standardized clinical data sheets and assess clinical situations Perform various administrative tasks on the computer Answering questions from parents and ...
... Data Management, Programming, Clinical Leadership, Project Physicians, and Medical Writing colleagues across Canada, Europe, the Americas, and AsiaPacific. Your Experience * Advanced degree in life ...
... Data Management, Programming, Clinical Leadership, Project Physicians, and Medical Writing colleagues across Canada, Europe, the Americas, and AsiaPacific. Your Experience * Advanced degree in life ...
... clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site ...
... clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site ...
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site ...
... clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site ...
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
... and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. * Per the Clinical Monitoring/Site Management Plan (CMP/SMP)
... clinical data integrity * Collaborate with Project Managers, fellow Business Analysts, and Implementation teams to coordinate timelines, resolve implementation challenges, and ensure successful go ...
... clinical data integrity * Collaborate with Project Managers, fellow Business Analysts, and Implementation teams to coordinate timelines, resolve implementation challenges, and ensure successful go ...
Clinical Data Manager information
See Quebec salary details
$20.43 - $25.72
4% of jobs
$25.72 - $31.01
5% of jobs
$31.01 - $36.30
9% of jobs
$40.43 is the 25th percentile. Wages below this are outliers.
$36.30 - $41.59
8% of jobs
$41.59 - $46.88
11% of jobs
The median wage is $51.94 / hr.
$46.88 - $52.16
12% of jobs
$52.16 - $57.45
15% of jobs
$60.54 is the 75th percentile. Wages above this are outliers.
$57.45 - $62.74
15% of jobs
$62.74 - $68.03
10% of jobs
$68.03 - $73.32
5% of jobs
$73.32 - $78.61
3% of jobs
$20
$52
$78
How much do clinical data manager jobs pay per hour?
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What Does a Clinical Data Manager Do?
A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).
What is a Clinical Data Manager?
What is the role of a Clinical Data Manager?
- What is the career path for Clinical Data Manager?
- What is the salary of Clinical Data Manager?
- What is the difference between Clinical Data Scientist and Clinical Data Manager?
- How to Become a Clinical Data Manager
- What Is a Clinical Data Manager and How to Become One
- Clinical Data Manager Job Description Sample Template
Full-time
Medical, Dental, Life, Retirement, PTO
Posted 5 days ago
Job description
Please refer to theHow to Apply for a Job (for External Candidates)job aid for instructions on how to apply.
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Position Summary:
The Data Manager will lead the development, implementation, and continuous improvement of research data management practices supporting the Clinical, Biospecimen, Imaging and Genetic (C-BIG) repository research initiatives focused on neurological diseases.
Reporting to the Senior Software Developer, the incumbent will provide leadership in the design, governance, and optimization of data management frameworks, standards, and operational workflows that support high-quality, secure, and accessible research data across multidisciplinary projects and collaborating institutions.
The Data Manager will act as a key resource for researchers, technical teams, and institutional stakeholders by promoting best practices in research data management, supporting interoperability between systems and platforms, and ensuring alignment with institutional policies, regulatory requirements, and strategic research priorities.
The role requires strong analytical, organizational, and communication skills, as well as the ability to exercise independent judgment, lead cross-functional initiatives, and manage complex data operations in a dynamic research environment.
Primary Responsibilities:
- Lead the development, implementation, and continuous improvement of research data management practices, standards, and operational workflows supporting repository and research activities
- Establish and oversee processes related to data governance, quality assurance, metadata standards, documentation practices, and lifecycle management for complex clinical and research datasets
- Engage researchers, technical teams, institutional stakeholders, and external collaborators to assess data management needs and identify opportunities to enhance operational effectiveness and data-sharing practices
- Identify, evaluate, and implement tools, platforms, and best practices that support secure, efficient, and scalable research data management workflows
- Promote the use of institutional platforms, shared resources, and standardized practices that support data accessibility, interoperability, and long-term sustainability
- Collaborate with software developers and research teams to support interoperability between new and existing systems, tools, databases, and repository infrastructure
- Ensure compliance with institutional policies, ethical requirements, privacy regulations, and applicable research data management guidelines
- Independently analyze and resolve complex data management and workflow issues while recommending and implementing sustainable process improvements
- Lead data validation, auditing, and quality monitoring activities to ensure data accuracy, completeness, consistency, and integrity across multiple research initiatives
- Develop and maintain standard operating procedures (SOPs), metadata documentation, data dictionaries, workflow documentation, and operational guidance materials
- Develop toolkits, training materials, and user resources that support researchers and staff in adopting effective data management and data-sharing practices
- Provide subject matter expertise and strategic guidance on research data management practices, repository operations, and data-sharing processes
- Collaborate with internal committees, working groups, and institutional partners on initiatives that support research data management priorities and operational objectives
- Foster collaborative relationships and communities of practice that promote knowledge sharing, continuous improvement, and alignment of data management approaches across teams
- Contribute to reports, operational analyses, presentations, and metrics used to support strategic planning, evaluation activities, and stakeholder communications
- Support onboarding, training, and guidance of students, trainees, and staff involved in repository data management activities
- Prepare meeting materials, take minutes, and follow up on action items
Other Qualifying Skills and/or Abilities
- Strong organizational skills with high attention to detail
- Ability to manage multiple tasks and deadlines in a research environment
- Clear written and verbal communication skills French and English
- Proficiency with common productivity tools (e.g., spreadsheets, document management systems, Github projects)
- Previous experience in a research, clinical, or academic setting
- Familiarity with neurological or neurodegenerative disease research
- Experience working with research databases or data capture tools
- Knowledge of data privacy, research ethics, or clinical study workflows
- Strong analytical and problem-solving skills
- Ability to collaborate effectively with multidisciplinary teams
- Adaptability and willingness to learn new tools and processes
- Professional discretion when handling sensitive research data
- Experience with mySQL preferred
As one of Montreal's Top Employers, here is what we offer:
- Competitive benefits package (Health, Dental, Life Insurance) (if eligible)
- Defined contribution pension plan (with employer contribution up to 10%) (if eligible)
- Group Registered Retirement Savings Plan (RRSP) and Tax Free Savings Account (TFSA)
- Competitive vacation policy
- Two (2) personal days
- Two (2) floating holidays
- Nine (9) "Summer Fridays" - paid days off between the St-Jean Baptiste holiday and Labour Day
- Paid time off over the December holiday period
- Tuition waiver for regular employees and their dependents
- Up to two (2) days of remote work per week where the position permits
Before applying, please note that to work at McGill University, you must be both authorized to work in Canada and willing to work in the province of Quebec at the campus where the position is based / located.
Knowledge of English: McGill University is an English-language university where day to day duties may require English communication both verbally and in writing. The level of English required for this position has been assessed at a level 4 on a scale of 0-4.
For a definition of our language proficiency levels, please click here.
Minimum Education and Experience:
Annual Salary:
Job Profile:
MPEX-IST2J - IT Analytics & Planning - Professional 2Hours per Week:
Supervisor:
Position End Date (If applicable):
Deadline to Apply:
McGill University hires on the basis of merit and is strongly committed to equity and diversity within its community. We welcome applications from racialized persons/visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and persons of minority sexual orientations and gender identities, as well as from all qualified candidates with the skills and knowledge to productively engage with diverse communities. McGill implements an employment equity program and encourages members of designated groups to self-identify. Persons with disabilities who anticipate needing accommodations for any part of the application process may contact, in confidence, accessibilityrequest.hr@mcgill.ca.