Clinical Project Manager
PSI CRO Open · verified Oct 24, 2026 At a glance
Manager-level role at PSI CRO. Remote, Canada · full-time · CA$135,000–CA$150,000 base.
remoteroles summary, based on the employer's posting.
What you'll do
- Run smaller phase II and III studies, keeping deliverables within agreed quality, timing and budget standards
- Take a regional lead or co-manager role on complex international programs and share responsibility for study outputs
- Lead project teams and coach clinical research staff, including CRAs and project coordination associates
- Contribute to feasibility work, proposals, client presentations and bid defense meetings
- Apply company procedures while maintaining service standards in customer interactions
What you bring
- A bachelor's degree, or equivalent preparation that includes at least five years in pharmaceutical or healthcare clinical research
- At least five years of clinical research industry experience, including two recent years as a project manager or equivalent
- Regional project management experience covering clinical study services from startup through closeout
- Strong written and spoken communication skills for building relationships with internal and external stakeholders
Who this fits
This is a manager-level role for someone ready to lead clinical research projects and teams, with hands-on responsibility across study delivery. The position is remote. Oncology, gastroenterology or radiopharmaceutical experience is a plus.
From the employer
PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.
Your responsibilities will include:
- Managing small (<5 countries and/or limited services) projects under direct or general supervision, with primary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget
- Performing regional lead’s or project co-manager’s role in complex international projects/programs with the secondary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget.
- Adhering to and promoting principles of delivery and service in dealing with PSI customers.
- Leading project teams
- Training, mentoring, and coaching Lead CRAs, Senior CRAs, CRAs, Project Coordination Associates (PCAs) and Site Management Associates (SMAs)
- Participating in feasibility research
- Supporting business development tasks such as proposals, client presentations, bid defense meetings, etc.
- Implementing company standard practices and complying with intradepartmental procedures
- Bachelor's degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities. Equivalency is defined as a minimum 5 years of experience gained in pharmaceutical/healthcare industry and clinical research.
- At least 5-year industry experience in clinical research
- At least 2-year recent clinical research experience in the capacity of project manager/equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.).
- Regional clinical project management experience, including management of all project services from startup to closure
- Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus
- Excellent communication skills, both written and verbal, with the ability to build strong internal and external stakeholder relationships
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
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