Clinical Project Manager

Job description

• Ensure the 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 of project plans to assure consistency with project goals
• Organisation and facilitation of project meetings related to study activities (study organization, initiation, execution, closure)
• 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 defence activities 
• Reference: SgmudfXIkrFpT3LyuL_vHKD-g9bDGh2Rc9rRgb6vCJk4MQSx-A0RGdJFaUxfuicD

Qualifications

• Experience of managing international clinical trials in a CRO environment
• Ideally knowledge of oncology, rare disease trials and / or complex studies
• Experience in selecting and managing external service providers
• Strong analytical, organisational, communication and numeracy skills
• Experience in CRO Industry
• Bachelor’s degree in a science related discipline.