remote job
Research & Academia
Remote
Sponsorship Not Stated
Join our Talent Pool - Clinical Research Associates (Canada)
Verified OpportunityChecked by PathwayAI staff.
Role Summary
Join Alimentiv's talent pool for future Clinical Research Associate roles in Canada, with opportunities for growth in clinical monitoring.
About the Organisation
As above, with the addition of the following:
- Clinical Research Associate I/II
- Support/conduct (as appropriate) site management through remote and supervised onsite visits (initiation, monitoring, and close-out) in compliance with SOPs, protocol, and GCP
- Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance
- Assist/lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle
- Support/conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support
- Maintain accurate, timely, and complete TMF documentation, requesting updates as required
- Provide day-to-day operational support to Senior CRA, and Lead CRAs
- Participate in training, study meetings, and CRA development activities, building competencies required for role progression
- Sr. Clinical Research Associate
- Act as subject matter expert, mentor, coach and/or provide performance feedback to manager for peers
- Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs.
- When required, act as the first escalation point for the resolution of site/patient issues or to address Sponsor concerns
- May represent Director, Monitoring and Site Management or Manager, Clinical Site Management in BD initiatives with a site monitoring focus
- May be assigned Lead CRA role and manage monitoring services for a group of projects and/or CRAs on large/complex project(s) including directing/guiding day to day activities and review/approval of monitoring reports
- Oversee overall integrity of the study to promote positive working relationships with the site and staff
- Ensure SOPs in place to optimize patient recruitment providing guidance to site teams of inclusion/exclusion criteria
Minimum Requirements
- CRA I - minimum 1 year experience + Honours Bachelor Degree
- CRA II - Minimum 2 years experience + Honours Bachelor Degree
- Sr. CRA - Minimum 3 years experience + Honours Bachelor Degree
Working Conditions
- Compensation may vary depending on the role seniority, geographic location, and candidate experience
- All full-time, permanent roles will include a base salary + elgibility for performance-based bonus, as well as a variety of health, dental, RRSP matching, and more!
- If contacted for an initial call, a member of our TA team will be happy to share more
Eligibility Criteria
Candidates are encouraged to join the talent pool for future opportunities, but there are no specific requirements mentioned regarding eligibility.
Exp. LevelNot specified
EducationNot specified
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