Project Manager II, Early Phase
- Canada
Full-time
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Job details
- Job type
- Full-time
- Posting language
- English
- Posted
Original job description
This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Project Manager II, Early Phase based in Canada.
Are you an experienced clinical research professional ready to lead complex early-phase clinical trials from initiation through closeout? This role offers the opportunity to oversee Phase I and II studies, ensuring projects meet their objectives, timelines, budgets, and quality standards. You will serve as a key point of contact for sponsors, vendors, clinical sites, and cross-functional teams, driving effective collaboration throughout the trial lifecycle. Working in a dynamic clinical research environment, you will manage resources, mitigate risks, and uphold regulatory compliance and patient safety. You will also contribute to process improvement, team development, and operational excellence. This is an opportunity to make a meaningful impact on clinical trial delivery while collaborating with talented professionals in a growing, innovation-driven organization.
How Jobgether Works
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Why Apply Through Jobgether?
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
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.
Are you an experienced clinical research professional ready to lead complex early-phase clinical trials from initiation through closeout? This role offers the opportunity to oversee Phase I and II studies, ensuring projects meet their objectives, timelines, budgets, and quality standards. You will serve as a key point of contact for sponsors, vendors, clinical sites, and cross-functional teams, driving effective collaboration throughout the trial lifecycle. Working in a dynamic clinical research environment, you will manage resources, mitigate risks, and uphold regulatory compliance and patient safety. You will also contribute to process improvement, team development, and operational excellence. This is an opportunity to make a meaningful impact on clinical trial delivery while collaborating with talented professionals in a growing, innovation-driven organization.
How Jobgether Works
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Why Apply Through Jobgether?
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
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.
More about this job
Responsibilities
Lead Phase I and II clinical trials from initiation through closeout, ensuring objectives, timelines, budgets, and quality standards are met. Coordinate sponsors, vendors, clinical sites, and cross-functional teams while managing resources and risks and maintaining regulatory compliance and patient safety.
Requirements
The posting indicates a mid-senior-level role for an experienced clinical research professional, with the capability to lead complex early-phase trials. It does not specify formal education, certifications, or a minimum number of years of experience.
Skills
- Clinical Trial Project Management
- Early-Phase Clinical Trials
- Phase I and II Studies
- Project Planning
- Budget Management
- Timeline Management
- Sponsor Relationship Management
- Vendor Management
- Clinical Site Coordination
- Cross-Functional Collaboration
- Resource Management
- Risk Mitigation
- Regulatory Compliance
- Patient Safety
- Process Improvement
- Team Development
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Management & Leadership
- Science & Research
Keywords
- Clinical Research
- Clinical Trials
- Early Phase
- Phase I
- Phase II
- Trial Lifecycle
- Project Initiation
- Project Closeout
- Project Objectives
- Timelines
- Budgets
- Quality Standards
- Sponsors
- Vendors
- Clinical Sites
- Cross-Functional Teams
- Resource Management
- Risk Mitigation
- Regulatory Compliance
- Patient Safety
- Process Improvement
- Team Development
- Operational Excellence