Key skills
Communication
About this role
Role Overview
- 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
- 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
- Training and career development opportunities internally
- Strong emphasis on personal and professional growth
- Friendly, supportive working environment
- Opportunity to work with colleagues based all over the world, with English as the company language