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ERGOMED

Project Manager, Senior – Oncology Experience Required

ERGOMED

Project Manager leading international clinical trials for oncology and rare diseases at Ergomed. Ensuring timely project delivery within budget and quality standards while collaborating with global teams.

Posted 7/29/2026full-timeRemote • 🇦🇷 ArgentinaSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing international clinical trials within a CRO environment, ensuring project delivery aligns with quality standards, timelines, and budgets. Proficient in developing project plans, facilitating meetings, and liaising with stakeholders while maintaining compliance with regulatory standards.

Highest-signal resume keywords
Project ManagementInternational Clinical TrialsOncology KnowledgeRegulatory ComplianceAnalytical 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 SkillsAnalytical Skills
Certifications & Qualifications
Bachelor’s Degree in Science
Industry Keywords
CROOncologyRare DiseaseBid DefenseStudy Activities

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
  • 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
  • We value teamwork, flexibility and a real commitment to work-life balance
  • Collaborative, international team