Markham, On Manager for clinical trials Jobs – 17 Openings This Week

Sr. Clinical Operations Lead (Clinical Trial Manager)
Alimentiv —Toronto, ON
- $78,000–$130,000 a year
- Full-time
- Remote
- Microsoft Office
- Bachelor's
- Organizational skills
Quick apply
Clinical Data Manager
Everest Clinical Research —Markham, ON
- $60,000–$90,000 a year
- Remote
- Doctoral degree
- Master's degree
- Databases
- Disability insurance
- Dental care
Quick apply
Senior Clinical Data Manager
Everest Clinical Research —Markham, ON
- $90,000–$130,000 a year
- Remote
- Master's degree
- In-person
- Disability insurance
- Dental care
Quick apply
Manager, Clinical Data Management
Everest Clinical Research —Markham, ON
- $140,000–$170,000 a year
- Remote
- Bachelor's
- In-person
- Disability insurance
- Dental care
Quick apply
Senior Clinical Trial Manager
Sitero LLC —Markham, ON
- Full-time
- Hybrid work
- Bachelor's
- Paid time off
Quick apply
1d
Clinical Team Lead, Phase I
Fortrea —Toronto, ON
- Weekends as needed
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Disability insurance
- Dental care
5d
Manager, Clinical Research Services
Michael Garron Hospital —Toronto, ON
- Full-time
- Research
- Supervising experience
- Bachelor's
Principal Data Manager I
Everest Clinical Research —Markham, ON
- $130,000–$165,000 a year
- Remote
- Master's degree
- Presentation skills
- Bachelor's
- Disability insurance
- Dental care
Quick apply
Clinical Data Collection Manager
Oncoustics —Toronto, ON
- Full-time
- Master's degree
- Databases
- Bachelor's
Lead Clinical Research Associate
PSI CRO —Toronto, ON
- $124,000–$153,000 a year
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's
Quick apply
22h
Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech
IQVIA —Toronto, ON
- $116,300–$193,800 a year
- Full-time
- Project management
- Bachelor's
Site Network Manager (North America)
Alimentiv —Toronto, ON
- $97,500–$163,000 a year
- Full-time
- Remote
- Nursing
- Bachelor's
- Travel
Quick apply
Commercial Partnerships & Alliances Lead
Novartis —Toronto, ON
- $128,240–$178,027 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Business development
- Analysis skills
5d
Chef d’équipe des données (Data Team Lead)
IQVIA —Toronto, ON
- $104,700–$154,700 a year
- Full-time
- Remote
- English
- Bachelor's
- Training & development
Lead, Health Economics & Outcomes Research
Novartis —Toronto, ON
- Full-time
- Hybrid work
- Research
- Analysis skills
5d
Bench Supervisor (Microbiology) - Eurofins BioPharma Product Testing Toronto, Inc.
Eurofins Canada BioPharma —Toronto, ON
- $65,000 a year
- Overtime
- Doctoral degree
- Laboratory experience
- Microsoft Office
- Designated paid holidays
- Disability insurance
Quick apply
Performance Analytics Reporting & GenAI Lead
Novartis —Toronto, ON
- $134,606–$186,865 a year
- Full-time
- Hybrid work
- SQL
- AI
- Python
12d

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Senior Clinical Data Manager
Everest Clinical Research —Markham, ON
Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical…
$90,000–$130,000 a year
Quick apply
Clinical Data Manager
Everest Clinical Research —Markham, ON
A Bachelors’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields with at least 2 years experience in clinical trial data…
$60,000–$90,000 a year
Quick apply

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manager for clinical trials jobs near markham, on

Sr. Clinical Operations Lead (Clinical Trial Manager)

Alimentiv -
Toronto, ON

Quick apply

Job details

Permanent | Full-time
$78,000–$130,000 a year

Qualifications

Microsoft Office
Bachelor's
Organizational skills
College diploma
Communication skills

Full job description

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and recruitment strategies, preparation of the monitoring plan and other structural documentation and the oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team.

Project Oversight

Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines.
Monitoring support visits (Co-monitoring), per project requirements, to aid the site/CRA in the satisfactory performance and compliance with standards mentioned above.
May support clinical project team by providing oversight of study deliverables related to other departments (e.g. Data Management, TMF Operations, etc.)
Oversee regional startup and feasibility activities.
Assist in vendor management activities as required per project.
Perform review of visit reports for quality, compliance and appropriate site management.
Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan.
Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc.) and inform clinical project team on progress.
Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site pass-through expense review.
May be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis.

Project Liaison

Conduct regular global CRA calls with the monitoring and site management team, as well as individual/country CRA calls
Attend meetings with Study Sponsor to provide status updates on country and site progress
Provide operational support and guidance to the monitoring team throughout project.
Provide project training/mentoring to regional CRAs on study procedures, clinical plans and guidelines, and timelines for the study. Ensures study specific training requirements are completed and documented.
First point of contact for regional CRAs for study-specific questions and issues. Escalates to PM and other functions as appropriate.
Support line managers by providing status updates on utilization and performance of CRAs.
Liaise with line manager for assigning sites to CRAs following line manager allocation of a CRA resource to the project.
Conduct CRA Assessment visits per departmental requirements to assess the performance of the CRA against their monitoring responsibilities.

Study Documents and Plans

Develop training materials and study tools for sites and CRAs, including monitoring plans.
Develop and implement enrolment and recruitment strategies together with clinical project team.
Develop presentation materials for and presents at Sponsor Kickoff meetings, Investigator meetings and Sponsor Calls (as needed), and prepares presentations for Site Qualification Visits and Site Initiation Visits.

Qualifications

College diploma/degree AND 7-9 years related experience +continuous training and knowledge/skills upgrading

Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial on-going job-related training

Other

Health Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation.
Should have a minimum of 3 years CRA experience, have strong experience with EDC systems, be proficient with MS Office, have strong written and verbal communication skills and highly effective interpersonal and organizational skills.
Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized.
Demonstrate the critical elements of GCPs and local regulations as they relate to clinical monitoring, IRB/EC and Investigator responsibilities.
Demonstrated ability in report writing and strong ability to critically understand clinical research documents.
Ability to handle multiple tasks to meet deadlines in a dynamic environment.

Working Conditions

Home-based

+ Bonus

Accommodations for persons with disabilities are available on request in respect of all aspects of the recruitment and selection lifecycle. Requests can be directed to [email protected]

PHISHING SCAM WARNING: Alimentiv is aware of the continued increase of phishing scams, leveraging various methods of attack via email, text, voice and social media. Please note that Alimentiv only uses company email addresses, which contain “@alimentiv.com”, to communicate with candidates via email. If you are contacted by someone about an open job at Alimentiv, please verify the domain of the sender’s email address and that they are asking you to apply on this website. If you believe you’ve been a victim of a phishing scam, please contact your local government cyber authority to report.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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Refine Your Search

manager for clinical trials jobs in markham, on

Sr. Clinical Operations Lead (Clinical Trial Manager)

Clinical Data Manager

Senior Clinical Data Manager

Manager, Clinical Data Management

Senior Clinical Trial Manager

Clinical Team Lead, Phase I

Manager, Clinical Research Services

Principal Data Manager I

Clinical Data Collection Manager

Lead Clinical Research Associate

Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech

Site Network Manager (North America)

Commercial Partnerships & Alliances Lead

Chef d’équipe des données (Data Team Lead)

Lead, Health Economics & Outcomes Research

Bench Supervisor (Microbiology) - Eurofins BioPharma Product Testing Toronto, Inc.

Performance Analytics Reporting & GenAI Lead

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