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Project Manager, Sr. Project Manager – Oncology Experience Required
ERGOMEDProject Manager overseeing delivery of oncology clinical trials at Ergomed clinical research organization. Managing project timelines, budgets, and stakeholder communication for successful outcomes.
Core Competencies
Role fitCore 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
Tailor your resumeApplicant 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