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ERGOMED

Project Manager, Sr. Project Manager – Oncology Experience Required

ERGOMED

Project Manager overseeing delivery of oncology clinical trials at Ergomed clinical research organization. Managing project timelines, budgets, and stakeholder communication for successful outcomes.

Posted 7/29/2026full-timeRemote • 🇨🇦 CanadaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing international clinical trials within a CRO environment, ensuring project delivery aligns with regulatory standards and quality expectations. Proficient in project planning, stakeholder communication, and training development to support study activities.

Highest-signal resume keywords
Project ManagementInternational Clinical TrialsOncology KnowledgeRegulatory StandardsAnalytical Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project PlanningBudget ManagementScope ManagementSOP DevelopmentTraining Program Development
Soft Skills
Organizational SkillsCommunication SkillsLiaison SkillsFacilitation Skills
Certifications & Qualifications
Bachelor’s Degree in Science
Industry Keywords
CRORare DiseaseBid DefenseStudy ActivitiesEC/IRB

About the role

Key responsibilities & impact
  • Ensure that projects are delivered on time, within budget, and agreed scope, maintaining the appropriate industry, sponsor and Ergomed quality standards
  • Liaise with project team members, provide training where needed and ensure correct allocation to tasks
  • Develop, review and edit project plans to assure consistency with goals and milestones
  • Organization and facilitation of project meetings related to study activities (study organization, initiation, execution, closure)
  • Serve as primary point of contact with sponsor and Ergomed Senior Management on project status
  • Represent Ergomed at external meetings, providing liaison with scientific/medical experts in other CRO/Sponsor companies and for committee meetings, (e.g.EC/IRB)
  • Develop review and edit of relevant SOPs to assure consistency with Regulatory standards and develop study related training programs to support this.
  • Contribute to bid defense activities

Requirements

What you’ll need
  • Experience serving as a Project Manager of international clinical trials in a CRO environment
  • Knowledge of Oncology and Rare Disease therapeutic areas
  • Experience in selecting and managing external service providers
  • Strong analytical, organizational and communication skills
  • Bachelor’s Degree in a science related discipline.

Benefits

Comp & perks
  • flexible work arrangements
  • professional development